125781308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5 prime UTR variant
orthologous variants: 30686300-G-T

125781326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5 prime UTR variant
orthologous variants: 30686279-C-T

125781379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 30686245-T-C

http://identifiers.org/hco/6/GRCh38#125781406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30686218-C-A

125781513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30686114-A-G

125781547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30686082-T-C

125782033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30685635-G-T

125782209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30685470-G-T

125782392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30685100-A-G

125782512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30684980-G-T

125782808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30684713-A-G

125786066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30682351-G-T

125786124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30682278-T-G

http://identifiers.org/hco/6/GRCh38#125787189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30681760-C-A

125787830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30681173-T-C

125787889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30681118-C-T

125787915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30681092-T-C

125788130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30680904-C-T

125788511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30680454-T-C

125788540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30680425-C-G

125788540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30680425-C-T

125789633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30680182-T-C

125789692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30680123-T-G

125789693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30680122-T-C

125789745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30680073-T-G

125789750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30680068-A-G

125789828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30679993-A-T

125789954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30679887-G-C

125790350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30679475-G-C

125790381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30679446-C-G

125790417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30679431-G-A

125790522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30679335-C-T

125790536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30679321-G-A

http://identifiers.org/hco/6/GRCh38#125790889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30679004-C-A

125790889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30679004-C-T

http://identifiers.org/hco/6/GRCh38#125790898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30678995-C-A

125790898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30678995-C-G

125790898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30678995-C-T

http://identifiers.org/hco/6/GRCh38#125790938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30678953-C-A

125790938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30678953-C-G

125790938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30678953-C-T

125790939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30678952-T-A

125790939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30678952-T-C

125791102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30678787-G-A

125791102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30678787-G-T

http://identifiers.org/hco/6/GRCh38#125791103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30678786-C-A

125791103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30678786-C-G

125791103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30678786-C-T

125791186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30678740-C-T

125791393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30678538-A-G

125791973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30677988-T-G

125792570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30677394-C-G

125793569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30675882-C-T

125793834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30675615-C-T

125793907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30675548-G-C

125794031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30675410-A-G

125794345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30675102-T-C

125794591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30674850-A-T

http://identifiers.org/hco/6/GRCh38#125794768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30672827-C-A

125794768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672827-C-T

125794822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672752-G-A

http://identifiers.org/hco/6/GRCh38#125794829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30672745-C-A

125794919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672679-A-G

125795177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672410-T-G

http://identifiers.org/hco/6/GRCh38#125795202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30672383-A-C

125795536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672142-C-T

125795592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672098-C-T

125795608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672082-G-A

125795608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672082-G-C

125795676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672029-C-T

125796011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30671733-G-C

125796977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30671241-G-A

125797595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30667048-T-G

125797733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30666912-G-T

125797770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30666875-G-A

125797770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30666875-G-C

125797770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30666875-G-T

125797891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30666785-T-A

125797891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30666785-T-C

125797919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30666757-A-G

125797919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30666757-A-T

125797947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30666718-A-G

125798138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30666514-G-A

125798361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30666353-A-G

125798720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30665954-C-T

125798730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30665944-A-G

125799825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30665345-C-T

125799948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30665225-G-A

125800083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30665092-G-A

125800227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30664965-G-A

125800265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30664927-C-T

http://identifiers.org/hco/6/GRCh38#125800506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30664682-A-C

125800507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30664681-A-G

125800576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30664497-T-C

125800614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30664346-G-C

125800720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30664246-A-G

125800854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30664121-C-G

125801152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30663836-G-A

125801169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30663822-A-G

125801222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30663773-A-G

125801806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30663034-A-G

125801808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30663032-C-T

125801971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30662858-A-G

125802103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30662735-G-A

125802103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30662735-G-T

http://identifiers.org/hco/6/GRCh38#125802269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30662576-C-A

125802269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30662576-C-T

125802281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30662563-T-C

http://identifiers.org/hco/6/GRCh38#125802418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30662466-C-A

125802418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30662466-C-T

125802423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30662461-T-C

125802461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30662435-A-G

125802495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30662401-G-T

http://identifiers.org/hco/6/GRCh38#125809754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30652342-A-C

125809754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30652342-A-G

125809846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30652266-T-C

125810129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30652196-C-T

125810243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30652159-G-T

125810274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30652122-T-G

125810549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30651859-T-G

125810844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30651563-T-G

125810920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30651481-T-C

125811331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30651025-A-G

125811689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650705-C-T

125811791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650604-T-C

125812149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650287-A-G

125812155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650281-A-G

125812199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650250-G-A

125812382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650121-T-C

125812687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649868-C-T

125812790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649785-T-C

125812790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649785-T-G

125814476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648588-A-G

125814673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648423-T-A

125814878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648245-C-T

125814897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648227-A-G

125815009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648109-G-A

125815009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648109-G-C

http://identifiers.org/hco/6/GRCh38#125815106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30648023-A-C

125815106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648023-A-G

125815226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30647901-T-C

125815364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30647763-A-G

125815462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647649-T-A

125815462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647649-T-C

125815462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647649-T-G

125815463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647648-T-G

http://identifiers.org/hco/6/GRCh38#125815554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30647594-C-A

125815758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647431-A-G

125815828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647386-G-A

125815830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647384-A-G

http://identifiers.org/hco/6/GRCh38#125816302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30647025-C-A

125816354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646981-G-A

125816424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646911-A-G

125816474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646862-T-G

125816481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646855-A-G

125816526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646809-A-G

125816576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646763-T-C

125816614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646725-C-T

125816626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646713-G-A

125816689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646652-G-C

125816870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646449-A-G

http://identifiers.org/hco/6/GRCh38#125816960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30646358-C-A

125816960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646358-C-T

125817378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645928-C-G

125818155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645261-T-C

125818300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645129-G-A

125818347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645094-A-G

125818425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645017-T-G

125818550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644831-A-G

125819341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30643924-A-G

125820242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30639258-G-A

125820884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30638614-A-G

125820884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30638614-A-T

125820885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30638613-T-C

125820896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30638601-C-G

125820896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30638601-C-T

125820928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30638567-G-T

125821059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30638454-C-T

http://identifiers.org/hco/6/GRCh38#125821135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30638387-C-A

125821169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30638353-A-T

125821171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30638351-G-A

125821534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30636819-C-T

125821847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30636537-C-T

125823171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30635941-A-G

http://identifiers.org/hco/6/GRCh38#125823323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30635791-A-C

125823323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30635791-A-G

125823331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30635783-G-C

125823484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30635658-G-A

125823657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30635495-T-A

125825518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30630330-T-C

http://identifiers.org/hco/6/GRCh38#125825525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30630323-C-A

125825614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30630235-G-A

125826687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30628621-T-C

http://identifiers.org/hco/6/GRCh38#125827533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30628490-C-A

125827598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30628421-C-G

125827946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30628083-C-T

125828031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30627985-T-C

125828052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30627964-C-G

125828052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30627964-C-T

125828112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30627901-C-T

125828249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30627766-G-T

125828284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30627728-C-T

125828443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30627173-G-A

125828587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30627038-T-C

http://identifiers.org/hco/6/GRCh38#125828693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30626948-A-C

125828868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30626767-T-C

125828869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30626766-T-C

125828995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30626639-C-T

125829533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30626106-T-C

125829701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30625924-C-T

http://identifiers.org/hco/6/GRCh38#125829730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30625900-A-C

125829731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30625899-T-G

125829878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30625792-G-A

http://identifiers.org/hco/6/GRCh38#125830099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30625591-A-C

125832194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30624090-A-G

125832325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30623972-A-G

125832337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30623960-A-G

125832443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30623870-C-T

125832488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30623816-C-G

125832641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30623697-C-G

125832641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30623697-C-T

125832785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30623561-A-G

125832931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30623423-C-G

125832931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30623423-C-T

http://identifiers.org/hco/6/GRCh38#125833811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30622833-A-C

125833969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30622699-G-A

125833969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30622699-G-T

125834230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30622248-C-T

125834269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30622211-A-G

125835243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30621682-A-G

125835243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30621682-A-T

125835595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30621375-G-C

125835765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30621194-G-A

125835951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30620873-T-A

http://identifiers.org/hco/6/GRCh38#125835995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30620829-C-A

125835995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30620829-C-T

125836253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30620550-C-T

125836325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30620478-T-C

http://identifiers.org/hco/6/GRCh38#125836335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30620468-A-C

125836417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30620384-C-G

125836755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30620095-A-G

125836868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30619847-T-A

125837078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30619661-A-G

125837190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30619404-A-G

125837269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30619321-A-G

125837536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30618687-C-G

125837541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30618682-T-C

125837848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30618194-G-A

125842376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30614278-C-T

125842837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30613041-T-C

125842909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30612980-T-C

125843001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30612722-G-A

125843266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30612387-G-T

125843318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30612341-A-G

125843318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30612341-A-T

125843366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30612296-G-C

125843399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30612263-G-T

125843471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30612001-T-C

125843866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30611485-A-G

125844395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30610536-G-C

125844396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30610535-C-G

125844396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30610535-C-T

125844806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609732-A-T

http://identifiers.org/hco/6/GRCh38#125845091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30609468-C-A

125845298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609275-G-A

125845315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609258-G-A

125846261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608120-C-T

125846334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608048-T-C

125846377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608023-T-C

125846430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30607971-T-C

125849542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30602602-T-C

125849767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30602375-G-A

125849825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30602319-T-G

125850063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601983-C-T

http://identifiers.org/hco/6/GRCh38#125850541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30601498-C-A

125850541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601498-C-T

125850546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601493-A-G

125850706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601343-G-A

125850744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601297-G-T

125851040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601004-A-G

125851076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30600968-A-G

125854440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30599726-G-A

125854546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30599641-C-G

125854546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30599641-C-T

http://identifiers.org/hco/6/GRCh38#125854722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30599470-A-C

125854963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30598893-A-G

125854995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30598881-T-C

125855013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30598867-T-C

125855014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30598866-T-C

http://identifiers.org/hco/6/GRCh38#125855105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30598775-A-C

125855105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30598775-A-T

125855133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30598747-G-A

125855133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30598747-G-T

125855254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598626-G-A

125855254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598626-G-T

125855256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598624-G-A

125855256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598624-G-T

125855261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598619-T-C

125855287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598314-T-C

125855305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598296-T-A

125855305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598296-T-G

125855327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598274-T-C

125855424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598150-T-A

125855424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598150-T-C

125855559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30598018-G-T

125855646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30597946-G-T

http://identifiers.org/hco/6/GRCh38#125855718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30597913-C-A

125855718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30597913-C-G

125855718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30597913-C-T

125856142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30597444-G-A

125856230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30597377-G-A

125856758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596806-G-A

125856775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596797-C-T

125856798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596784-T-G

125857129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596487-T-A

125857913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596371-A-T

125858083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596209-G-T

125858268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595467-C-T

125859724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30594202-T-A

125860034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30593911-T-C

http://identifiers.org/hco/6/GRCh38#125860536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30593284-C-A

125860536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30593284-C-T

125860671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30593190-T-C

125860846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30593027-G-T

http://identifiers.org/hco/6/GRCh38#125863270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30590576-C-A

http://identifiers.org/hco/6/GRCh38#125863785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30590111-C-A

125863804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30590093-A-G

125863960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30589947-C-T

125864071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30589835-T-G

125865650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30588351-T-G

125871399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30584966-C-G

125871418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30584957-C-T

125871470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30584904-A-G

125871540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30584830-T-C

125871644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30584724-C-T

125872133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30583722-T-A

125872133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30583722-T-C

125872280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30583581-A-G

125872561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30583086-A-G

125872839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582795-G-A

125873072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582653-A-G

125873072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582653-A-T

125873248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582444-G-A

125873313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582374-T-C

125873549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582177-A-G

125873549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582177-A-T

125873593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582135-G-A

125873635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582094-G-A

125873635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30582094-G-C

125873916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30581910-C-T

125873931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30581895-G-A

http://identifiers.org/hco/6/GRCh38#125874065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30581790-C-A

125874381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30581175-G-A

125874541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30581029-T-A

125874739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30580823-T-G

http://identifiers.org/hco/6/GRCh38#125875013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30580548-A-C

125875013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30580548-A-G

http://identifiers.org/hco/6/GRCh38#125875053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30580508-C-A

125875080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30580481-C-G

125876033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30578726-A-T

http://identifiers.org/hco/6/GRCh38#125878137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30578162-C-A

125878137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30578162-C-T

125878138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30578161-T-A

125878229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30578067-T-C

125878306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30577977-A-G

125878466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30577816-A-G

125878684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576859-G-A

http://identifiers.org/hco/6/GRCh38#125878728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30576814-A-C

125878728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576814-A-T

125878875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576669-C-T

125878997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576615-T-A

125879110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576552-A-G

125879174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576487-T-C

125879257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576403-T-C

125879317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576362-T-C

125879398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576280-C-T

125879438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576243-T-C

125879487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30576194-G-A

125880086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30575557-G-A

125880161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30575499-G-A

125880218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30575449-T-C

125880302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30575402-T-C

125880304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30575400-C-T

125880870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30574446-A-G

125881053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30574273-T-C

125881235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30574084-A-G

125881268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30574064-A-T

http://identifiers.org/hco/6/GRCh38#125881269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30574063-C-A

125881286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30574045-G-A

125881286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30574045-G-T

http://identifiers.org/hco/6/GRCh38#125881338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30573981-C-A

125881338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30573981-C-T

125882404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30572208-T-C

125882404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30572208-T-G

125882558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30572055-A-G

125882558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30572055-A-T

125882563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30572050-T-A

125882563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30572050-T-C

http://identifiers.org/hco/6/GRCh38#125882649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30571978-C-A

125882649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571978-C-T

125882657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571970-G-A

125882661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571966-A-G

http://identifiers.org/hco/6/GRCh38#125882686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30571941-A-C

125882694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571933-T-G

125882751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571877-G-T

125882768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571860-T-C

125882947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571695-T-C

125882982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571660-T-A

125883050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571596-C-T

125884392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571361-C-T

125884586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571190-C-G

125884609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571167-A-G

125884687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571089-A-G

125884687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30571089-A-T

http://identifiers.org/hco/6/GRCh38#125884854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30570933-A-C

http://identifiers.org/hco/6/GRCh38#125885017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30570372-C-A

125885017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30570372-C-T

125885045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30570344-A-T

125885057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30570334-A-G

http://identifiers.org/hco/6/GRCh38#125885295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30570111-C-A

125885295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30570111-C-T

125885303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30570103-A-G

125885441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30569970-A-G

125885453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30569958-A-G

125885539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30569874-T-A

125886975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30569670-T-A

125887082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30569542-T-C

125887492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30569138-T-C

125887675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30568963-C-T

125888376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30568306-T-C

125888674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30568036-A-G

125888802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30567909-G-T

125888848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30567864-G-A

125888848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30567864-G-T

125889117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30567603-A-T

125889122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30567598-A-G

http://identifiers.org/hco/6/GRCh38#125889133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30567581-C-A

http://identifiers.org/hco/6/GRCh38#125889136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30567578-A-C

125889136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30567578-A-G

125889297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30567429-G-A

125889445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30567290-A-G

125889502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30567233-A-T

125889573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30567162-G-A

125889684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30567051-G-C

125889703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30567032-G-A

125889773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30566962-G-C

http://identifiers.org/hco/6/GRCh38#125889987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30566745-C-A

125889987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566745-C-T

125890008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566699-A-G

125890010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566697-A-G

125890010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566697-A-T

125890020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566677-A-G

125890041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566655-G-A

125890052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566644-A-G

125890064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566632-A-G

http://identifiers.org/hco/6/GRCh38#125890091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30566593-A-C

125890092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566592-A-G

125890092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566592-A-T

125890279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566396-T-G

125890411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566081-T-C

125890513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565979-C-T

125890551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565953-G-A

125890552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565952-A-G

125890603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565902-T-G

125890616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565889-G-A

125890616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565889-G-C

125890616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565889-G-T

125890677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30565831-C-G

125890677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30565831-C-T

125890797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30565711-G-A

125890797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30565711-G-C

125890797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30565711-G-T

125890907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565610-A-G

125890927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565590-A-G

125890942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565572-A-G

125890944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565570-A-G

http://identifiers.org/hco/6/GRCh38#125890948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30565566-A-C

125890948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565566-A-G

http://identifiers.org/hco/6/GRCh38#125891153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30565418-C-A

125891169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565402-A-T

125891216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565352-A-G

http://identifiers.org/hco/6/GRCh38#125891666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30564369-A-C

125891671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564364-A-G

125891717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564318-C-G

125891939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564098-T-C

125892221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30563752-C-T

125892393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30563586-G-A

125893266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30563055-G-C

125893393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30562755-T-G

125893851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30562321-G-T

125894002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30562167-T-G

125894010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30562159-T-C

125899204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30556717-A-G

125899304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30556616-A-G

125899546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30556276-T-G

125899623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30556202-T-C

125899629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30556196-T-G

http://identifiers.org/hco/6/GRCh38#125899677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30556134-A-C

http://identifiers.org/hco/6/GRCh38#125899857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#30555944-C-A

125899857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30555944-C-G

125904354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30555623-T-C

125904373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30555605-T-C

125904397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30555571-G-A

125904397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30555571-G-T

125904452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30555511-G-A

http://identifiers.org/hco/6/GRCh38#125904754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30554561-C-A

125904982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30554337-A-G

http://identifiers.org/hco/6/GRCh38#125905013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30554304-A-C

125905013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30554304-A-G

125905073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30554244-G-A

125905108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30554223-A-G

125905282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30554051-G-A

125905282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30554051-G-T

125906136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30553840-T-G

125906309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30553649-C-T

125906359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30553597-A-T

125906610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30553420-G-A

125906610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30553420-G-T

125906855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30553175-C-G

125906996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30553040-A-G

125907091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552950-G-A

125907230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552805-G-A

125907244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552800-C-T

125907430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552664-G-A

125907563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552533-A-G

125908045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552086-G-C

125908110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552029-A-G

125908342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30551441-A-G

125908374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30551391-C-T

125908384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30551381-C-T

125908591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30551182-A-G

125908655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30551111-C-T

125908772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30550989-T-C

125908887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30550882-C-T

125909322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30550495-T-G

125909361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30550460-G-T

125909977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549940-G-A

125910051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549891-T-A

125910188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549767-C-T

125910213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549742-G-A

125910229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549649-G-A

125910287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549606-C-G

125910344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549536-C-T

125910597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549290-T-G

125910722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549091-C-T

125914684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30539079-G-T

125914991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538784-C-T

125915104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538675-A-G

125915104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538675-A-T

125915294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538481-G-A

125915313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538455-G-A

125915313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538455-G-T

125915492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538276-G-T

http://identifiers.org/hco/6/GRCh38#125915515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30538246-C-A

125915515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538246-C-G

125915523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538230-A-G

http://identifiers.org/hco/6/GRCh38#125916389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30538089-C-A

125916389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538089-C-T

125916452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538028-T-C

125916456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30538024-C-T

125916598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30537838-G-A

125916769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30537668-G-A

http://identifiers.org/hco/6/GRCh38#125917398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30533043-C-A

125917431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30533008-G-A

125918237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30532837-T-C

125919076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30531991-T-C

125919127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30531949-A-T

125919157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30531920-T-A

125919157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30531920-T-C

125919290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30531764-G-A

http://identifiers.org/hco/6/GRCh38#125919312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#30531744-A-C

125919533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30531524-G-A

125919559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30531516-T-C

http://identifiers.org/hco/6/GRCh38#125919615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#30531468-C-A

125920097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30531058-T-A

125920201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30530971-A-G

125920221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30530946-T-G

125920250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30530922-T-G

125920361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30530823-T-A

http://identifiers.org/hco/6/GRCh38#125920829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30530546-C-A

125920829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30530546-C-G

125920829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30530546-C-T

125921006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30530373-G-A

125921028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30530345-G-A

125921028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30530345-G-C

125921039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30530334-G-A

125921159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30530288-T-C

http://identifiers.org/hco/6/GRCh38#125921189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30530278-C-A

125921189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30530278-C-T

125921835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529989-T-C

125922355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529536-C-T

125922422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529466-T-A

125922598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529162-T-A

125922603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529157-G-A

125922604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529156-G-A

125922604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529156-G-T

125922645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529116-G-A

125922645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529116-G-T

http://identifiers.org/hco/6/GRCh38#125922649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30529112-C-A

125922649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30529112-C-T

125922736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30529028-A-G

125922903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30528644-T-A

125922986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30528564-T-C

125922986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30528564-T-G

125923115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30528490-A-G

125923115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30528490-A-T

125923134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30528477-T-C

125923858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30527578-G-A

125923858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30527578-G-T

125924279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30527205-T-C

125924968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30526383-T-C

125924977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30526374-C-T

125926608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30525742-T-C

125926671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30525693-T-G

125927228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30525082-T-C

125927415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30524794-A-G

125927493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30524717-G-T

125927546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30524657-A-T

125927637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30524560-G-A

125927818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30524372-G-A

125927818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30524372-G-T

http://identifiers.org/hco/6/GRCh38#125927870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30524321-C-A

125927870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30524321-C-G

125927870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30524321-C-T

http://identifiers.org/hco/6/GRCh38#125927880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30524311-C-A

125928029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30524168-T-C

125928029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30524168-T-G

125928120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30524088-T-C

125928561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: intron variant
orthologous variants: 30523721-T-C

125928820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30523461-G-T

http://identifiers.org/hco/6/GRCh38#125928970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30523320-C-A

125928970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30523320-C-T

125929067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30523208-A-G

125929155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30523122-A-G

http://identifiers.org/hco/6/GRCh38#125929220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30523058-C-A

http://identifiers.org/hco/6/GRCh38#125929229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30523049-A-C

125929281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30523010-G-T

125929296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30522995-T-A

125930659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30521998-A-G

125930704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30521951-A-G

http://identifiers.org/hco/6/GRCh38#125930762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#30521893-C-A

125930910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30521774-A-G

125930986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30521698-C-T

125931118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30521570-T-C

http://identifiers.org/hco/6/GRCh38#125931378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#30520766-C-A

125931378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 30520766-C-T

125931424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30520724-G-A

125931424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30520724-G-T

125931475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30520684-G-A

125931475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30520684-G-T

125931507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21081
most severe consequence: 3 prime UTR variant
orthologous variants: 30520663-A-G