169987085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61129291-T-C

169987185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61129193-G-A

169987231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61129148-G-A

169987578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61128784-A-G

169987947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61128453-A-G

169988051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61128356-T-C

169988409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127983-G-T

169988429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127963-G-A

169988457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127926-T-C

169988472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127911-G-A

http://identifiers.org/hco/4/GRCh38#169988544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61127808-C-A

169988544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127808-C-T

169988682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127665-G-A

169988684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127663-A-G

169988705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127643-G-A

169988782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127570-G-A

169988782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127570-G-T

169988826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127526-T-G

169988891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127468-T-C

169988954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127406-G-A

169988954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127406-G-T

169988956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127404-T-C

169989013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127342-A-G

169989022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127333-G-A

169989022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127333-G-C

http://identifiers.org/hco/4/GRCh38#169989041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61127319-C-A

http://identifiers.org/hco/4/GRCh38#169989043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61127317-C-A

169989113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127249-A-G

169989182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127191-A-G

169989183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127190-T-C

169989189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127184-T-C

http://identifiers.org/hco/4/GRCh38#169989230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61127142-C-A

169989234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127138-G-A

169989234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127138-G-T

169989266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127108-T-C

169989311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127073-T-C

169989321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127063-T-A

169989321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61127063-T-C

http://identifiers.org/hco/4/GRCh38#169989344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61127040-A-C

169989427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126968-T-C

169989553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126848-G-T

http://identifiers.org/hco/4/GRCh38#169989566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61126835-C-A

169989566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126835-C-T

169989568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126833-C-G

169989582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126819-G-A

169989582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126819-G-T

169989609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126783-A-G

169989628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126767-A-G

169989645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126750-T-C

169989722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126682-A-G

http://identifiers.org/hco/4/GRCh38#169989737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61126656-C-A

169989737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126656-C-T

169989739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126654-T-C

169989814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126584-A-T

169989936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126465-T-C

169990059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126323-G-A

169990075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126307-A-G

169990163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61126216-T-C

http://identifiers.org/hco/4/GRCh38#169990323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61126087-C-A

169990664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61125717-G-A

169990898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61125478-T-C

169991235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61125128-G-A

169991252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61125111-G-T

169991487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124878-G-A

169991514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124851-G-C

http://identifiers.org/hco/4/GRCh38#169991520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61124845-A-C

169991577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124788-T-C

169991748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124617-T-C

169991799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124566-A-G

169991826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124539-A-G

169992078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124287-C-G

169992090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124275-C-T

169992156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124209-A-T

169992225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124140-G-C

169992225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61124140-G-T

169992303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 61124062-C-T

http://identifiers.org/hco/4/GRCh38#169992339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61124026-C-A

169992339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61124026-C-T

169992363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61124002-A-T

169992783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61123313-T-C

169992966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61123112-G-A

169993410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61122738-G-A

169993410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61122738-G-T

169993628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122476-A-G

169993653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122451-T-C

169993778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122326-C-T

169993789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122316-T-C

http://identifiers.org/hco/4/GRCh38#169993835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61122270-C-A

http://identifiers.org/hco/4/GRCh38#169993893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61122215-C-A

169993893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122215-C-T

http://identifiers.org/hco/4/GRCh38#169993903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61122202-C-A

http://identifiers.org/hco/4/GRCh38#169993932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61122173-C-A

169993932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122173-C-T

169993986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122124-G-C

http://identifiers.org/hco/4/GRCh38#169994055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61122059-A-C

http://identifiers.org/hco/4/GRCh38#169994056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61122058-A-C

169994056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122058-A-T

169994057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122057-T-C

http://identifiers.org/hco/4/GRCh38#169994061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61122053-C-A

169994061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122053-C-T

169994093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61122025-G-T

http://identifiers.org/hco/4/GRCh38#169994143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61121985-A-C

169994190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61121940-T-C

169994430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61121727-C-G

169994430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61121727-C-T

169994677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61121489-A-G

169994701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61121465-C-T

169994709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61121457-T-C

169994886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61121039-A-G

169994886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61121039-A-T

169994890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61121035-C-G

169995047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61120910-G-C

169995047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61120910-G-T

http://identifiers.org/hco/4/GRCh38#169995115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61120867-C-A

169995147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61120835-T-C

169995188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61120790-G-A

169995271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61120583-A-G

169995290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61120511-G-A

169995290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61120511-G-T

169995335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61120448-T-G

169996026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61119733-T-C

169996026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61119733-T-G

http://identifiers.org/hco/4/GRCh38#169996034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61119725-C-A

169996600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61119179-A-G

169996601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61119178-G-A

169996655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61119152-G-C

169996838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61118959-T-C

169996845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61118952-G-C

169996906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61118896-C-T

http://identifiers.org/hco/4/GRCh38#169997031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61118798-C-A

169997389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61118459-G-A

169997392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61118456-G-A

169997644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61118157-G-A

169998021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117946-A-G

169998147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117738-G-C

169998156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117729-G-C

169998258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117642-A-G

169998352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117549-C-T

169998364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117533-C-T

169998397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117500-C-T

169998403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117494-A-G

169998528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117381-C-G

169998633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117288-A-G

169998712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117212-A-T

169998739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117187-T-A

169998790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117143-A-G

169998923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117018-T-A

169998930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61117011-G-A

169998966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116981-T-C

169999162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116785-G-C

169999171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116776-C-T

169999176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116771-C-T

169999209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116743-T-C

169999223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116727-G-C

169999276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116674-A-T

169999290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116663-G-A

169999290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116663-G-C

http://identifiers.org/hco/4/GRCh38#169999731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61116230-A-C

169999812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116125-C-T

169999873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116064-T-C

169999918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61116030-G-C

170000019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61115921-G-T

http://identifiers.org/hco/4/GRCh38#170000076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61115860-C-A

170000076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61115860-C-T

http://identifiers.org/hco/4/GRCh38#170000083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61115853-A-C

170000408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61115145-G-A

170001024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61114810-T-G

170001433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61114256-C-T

170001451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61114230-C-T

170001461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61114220-T-C

170001524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61114164-G-A

170001618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61114058-T-C

170001729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113945-G-T

http://identifiers.org/hco/4/GRCh38#170001790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61113881-A-C

170001854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113813-G-A

170001875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113791-A-G

http://identifiers.org/hco/4/GRCh38#170001915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61113749-C-A

170001915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113749-C-T

170001939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113725-G-T

170001982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61113682-G-A

170002067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61113596-T-C

170002100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61113573-T-C

http://identifiers.org/hco/4/GRCh38#170002137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61113538-A-C

170002137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61113538-A-G

170002304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113372-T-C

http://identifiers.org/hco/4/GRCh38#170002322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61113354-C-A

170002323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113353-T-A

170002324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113352-G-A

170002324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113352-G-T

http://identifiers.org/hco/4/GRCh38#170002346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61113330-C-A

170002346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113330-C-G

170002346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113330-C-T

http://identifiers.org/hco/4/GRCh38#170002787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61113171-C-A

170002988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61113016-A-G

170003181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61112829-G-A

170003369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61112655-C-T

170003564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61112463-G-A

170003564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61112463-G-T

170003631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61112396-T-C

http://identifiers.org/hco/4/GRCh38#170003680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61112348-A-C

170003680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61112348-A-T

170003687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61112341-A-G

170003688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61112340-T-C

http://identifiers.org/hco/4/GRCh38#170003702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61112326-C-A

170003702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61112326-C-T

http://identifiers.org/hco/4/GRCh38#170003703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61112325-C-A

170004301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61111169-A-G

170004556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61110921-A-T

170004661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61110832-A-G

http://identifiers.org/hco/4/GRCh38#170004932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61110557-C-A

170005059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61110423-A-G

170005245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61110240-G-T

170005434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61110061-G-T

170005452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61110041-G-C

170005452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61110041-G-T

http://identifiers.org/hco/4/GRCh38#170005508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61109985-A-C

170005508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61109985-A-G

http://identifiers.org/hco/4/GRCh38#170005938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61109567-A-C

170005938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61109567-A-G

170005947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61109558-T-C

http://identifiers.org/hco/4/GRCh38#170006153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61109370-C-A

170006153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61109370-C-G

170006153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61109370-C-T

http://identifiers.org/hco/4/GRCh38#170006392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61109117-C-A

170006392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61109117-C-T

170006692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61108949-A-G

170006708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61108935-A-T

170006999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61108604-G-T

170007049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61108541-G-T

170007189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61104856-T-A

170007479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, undefined
orthologous variants: 61104578-G-A

http://identifiers.org/hco/4/GRCh38#170007541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61104532-C-A

170007914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61103971-T-C

170007915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61103970-T-G

170008105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61103789-G-C

170008455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61103463-C-T

170008529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61103390-G-C

170008572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61103362-T-C

170008775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61103213-T-C

170008777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61103211-C-T

170009088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61102929-T-C

170009896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61102421-G-A

170009899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61102418-T-C

170009974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61102343-T-C

170012176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61102089-T-C

170012355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61101914-G-C

170012647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61101660-G-C

170012647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61101660-G-T

http://identifiers.org/hco/4/GRCh38#170012755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61101569-C-A

170012846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61101462-G-A

170012943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61101366-T-G

170012977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61101338-C-T

170013253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61100872-G-C

170013301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61100824-G-A

170013551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61100589-G-A

http://identifiers.org/hco/4/GRCh38#170013641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61100516-C-A

170013641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61100516-C-T

170013870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61100342-T-C

170013875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61100337-T-C

170013894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61100320-G-A

170013969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61100252-A-G

170014005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61100217-C-T

170014293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61099282-A-G

170014362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61099205-A-T

170015044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61098138-A-T

170015069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61098115-T-G

170015137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61098051-T-C

170015274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61097916-C-T

170017285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61096841-A-G

170017519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61096622-C-T

170017587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61096561-T-C

170017848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61096033-T-G

170017939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61095947-A-T

http://identifiers.org/hco/4/GRCh38#170018066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61095826-A-C

http://identifiers.org/hco/4/GRCh38#170018167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61095776-A-C

170018331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61095612-T-C

170018615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61095320-A-G

170018700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61095235-A-G

170018734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61095202-C-T

170018882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61094696-G-A

170019624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61093922-T-A

http://identifiers.org/hco/4/GRCh38#170019837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61093695-C-A

170020093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61093494-T-C

170021435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61091687-G-A

170022009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61090911-T-C

170022025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61090895-C-T

http://identifiers.org/hco/4/GRCh38#170022067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61090849-C-A

170022179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61090274-A-G

170022512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61089364-T-C

170022524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61089352-G-A

170022534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61089342-G-A

170022544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61089332-G-A

170022544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61089332-G-C

170022918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61088496-A-G

170023038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61088383-G-C

170023084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61088333-A-G

170023782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61087646-T-C

170025196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61087098-T-G

170025215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61087079-C-T

170025263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61087029-G-A

170025263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61087029-G-C

170025707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086591-A-G

170025753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086545-G-A

170025763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086535-A-G

170025992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086316-A-G

170026002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086306-A-G

170026008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086300-C-T

170026073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086242-C-G

170026106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086219-C-T

170026173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086154-G-A

170026173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61086154-G-T

http://identifiers.org/hco/4/GRCh38#170026201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#61086127-C-A

170026267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 61086057-G-A

170026356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61085998-C-T

170026370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61085981-C-T

170026562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, undefined
orthologous variants: 61085786-G-A

170026562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, undefined
orthologous variants: 61085786-G-T

170026609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61085766-G-A

http://identifiers.org/hco/4/GRCh38#170026615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#61085760-C-A

170026615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, undefined
orthologous variants: 61085760-C-T

170026631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61085744-T-C

170026754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61085599-G-T

170026770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, undefined
orthologous variants: 61085583-A-G

170026814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, undefined
orthologous variants: 61085539-T-C

170026894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61085471-A-G

http://identifiers.org/hco/4/GRCh38#170026928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61085434-C-A

170026928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61085434-C-T

170026942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61085420-T-C

http://identifiers.org/hco/4/GRCh38#170026967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61085406-C-A

170026967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61085406-C-G

170026967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61085406-C-T

170027025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61085351-T-C

170027062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61085314-T-C

http://identifiers.org/hco/4/GRCh38#170027090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#61085288-A-C

170027090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61085288-A-G

170027207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61085169-C-G

170027207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 61085169-C-T

http://identifiers.org/hco/4/GRCh38#170027220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61085124-C-A

170027220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61085124-C-T

170027228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61085116-T-C

170027261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61085008-C-T

http://identifiers.org/hco/4/GRCh38#170027318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61084949-C-A

170027500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61084734-T-C

170027734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61084506-T-C

170028053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61084239-T-C

170028120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61084175-C-T

170028275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61084022-G-T

170028438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61083851-T-G

170028472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61083819-T-G

170028513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61083777-A-G

170028680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61083631-A-G

170029292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61083146-C-T

170029293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61083145-G-A

170029293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61083145-G-T

http://identifiers.org/hco/4/GRCh38#170029344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61083102-A-C

170029423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61083025-A-G

170029718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61082813-C-G

170029946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61082584-A-G

170029996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61082543-G-A

170030038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61082501-T-G

170031502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61080984-G-T

170031569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61080918-G-A

170031749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61080798-G-A

170031749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61080798-G-T

170031773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron variant
orthologous variants: 61080774-C-G

170031818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61080731-G-T

http://identifiers.org/hco/4/GRCh38#170031830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#61080727-C-A

170031928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61080705-A-G

170032000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61080671-G-A

170032494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61080486-G-A

170032577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61080416-A-G

170032850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: non coding transcript exon variant
orthologous variants: 61080220-G-T

170032954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: non coding transcript exon variant
orthologous variants: 61080135-A-T

170032963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: non coding transcript exon variant
orthologous variants: 61080126-G-A

170032963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29083
most severe consequence: non coding transcript exon variant
orthologous variants: 61080126-G-T