http://identifiers.org/hco/1/GRCh38#31179812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130341045-C-A

http://identifiers.org/hco/1/GRCh38#31179874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130340987-C-A

31179874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340987-C-G

31179902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340960-G-A

31179902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340960-G-T

http://identifiers.org/hco/1/GRCh38#31180003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130340859-C-A

31180003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340859-C-T

31180082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340785-T-C

31180107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340755-G-A

31180107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340755-G-T

31180126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340736-G-T

http://identifiers.org/hco/1/GRCh38#31180240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130340670-C-A

31180240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340670-C-T

31180282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340637-T-C

31180293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340624-T-C

31180305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340612-A-G

http://identifiers.org/hco/1/GRCh38#31180330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130340587-C-A

31180330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340587-C-G

31180414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340504-G-A

31180415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340503-G-A

31180415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3 prime UTR variant
orthologous variants: 130340503-G-T

http://identifiers.org/hco/1/GRCh38#31180587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130340406-C-A

http://identifiers.org/hco/1/GRCh38#31180608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130340395-C-A

31180608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130340395-C-T

31180612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130340391-T-C

31180639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130340364-G-A

31180828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130340180-T-A

31180828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130340180-T-C

31180850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130340161-G-T

31180905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130340102-T-C

31180933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130340082-G-A

31180952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130340063-C-G

31181126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130339908-T-A

31181126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130339908-T-C

31181126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130339908-T-G

31181199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130339831-A-G

31181199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130339831-A-T

31181212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130339818-T-C

31181240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 130339784-T-C

31181243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130339781-G-A

31181243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130339781-G-T

http://identifiers.org/hco/1/GRCh38#31181319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130339707-A-C

31181319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130339707-A-G

http://identifiers.org/hco/1/GRCh38#31181650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130339400-C-A

31181650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 130339400-C-T

31181653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 130339391-C-T

http://identifiers.org/hco/1/GRCh38#31181706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130339336-C-A

31181706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: synonymous variant
orthologous variants: 130339336-C-T

31181756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130339282-T-C

http://identifiers.org/hco/1/GRCh38#31181799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130339241-C-A

31181799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130339241-C-T

31181802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130339238-T-C

31181803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130339237-C-T

http://identifiers.org/hco/1/GRCh38#31181804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130339236-C-A

31181804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130339236-C-T

http://identifiers.org/hco/1/GRCh38#31181833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130339197-C-A

31181833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130339197-C-T

31181836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130339194-A-G

http://identifiers.org/hco/1/GRCh38#31181901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130339133-C-A

31181901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: synonymous_variant, undefined
orthologous variants: 130339133-C-T

31181995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130339066-G-A

31181995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130339066-G-C

31181995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130339066-G-T

http://identifiers.org/hco/1/GRCh38#31182005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130339056-C-A

31182005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130339056-C-T

31182246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338883-T-G

31182289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338863-T-G

http://identifiers.org/hco/1/GRCh38#31182379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130338776-C-A

31182379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338776-C-G

31182379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338776-C-T

31182395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338759-A-T

http://identifiers.org/hco/1/GRCh38#31182398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130338756-C-A

31182398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338756-C-G

31182398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338756-C-T

http://identifiers.org/hco/1/GRCh38#31182449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130338713-C-A

31182449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338713-C-G

31182449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338713-C-T

31182599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338571-G-T

http://identifiers.org/hco/1/GRCh38#31182665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130338477-A-C

31182665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338477-A-G

http://identifiers.org/hco/1/GRCh38#31182674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#130338462-C-A

31182674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338462-C-G

31182674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338462-C-T

31182684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130338448-A-G

31182992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130338041-C-T

http://identifiers.org/hco/1/GRCh38#31183021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130338012-A-C

31183136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337909-T-G

31183520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337565-C-G

31183634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337464-G-C

http://identifiers.org/hco/1/GRCh38#31183723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130337423-C-A

31183723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337423-C-T

31183725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337421-G-A

31183725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337421-G-T

31183795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337415-G-C

31184034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337178-G-A

31184034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337178-G-T

31184092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337091-T-A

31184092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130337091-T-C

31184107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: -G-A

31184107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: -G-T

31184127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130337061-T-C

http://identifiers.org/hco/1/GRCh38#31184226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130336963-C-A

31184756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334459-G-C

http://identifiers.org/hco/1/GRCh38#31184804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130334389-C-A

31184804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334389-C-T

http://identifiers.org/hco/1/GRCh38#31184815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130334378-C-A

31184815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334378-C-T

31185015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334203-G-A

31185015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334203-G-C

31185015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334203-G-T

31185052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334166-G-A

31185052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334166-G-T

31185137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334074-G-A

31185137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334074-G-T

31185158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130334052-A-T

31185210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130334018-G-T

31185399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130333829-G-A

31185399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130333829-G-T

http://identifiers.org/hco/1/GRCh38#31185417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130333817-C-A

31185417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130333817-C-T

31185565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130333728-T-A

http://identifiers.org/hco/1/GRCh38#31187503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130332606-A-C

31187650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130332481-A-G

http://identifiers.org/hco/1/GRCh38#31187851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130332328-C-A

31187851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130332328-C-T

31187902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130332294-G-A

31187902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130332294-G-T

31187930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130332280-T-C

31187956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130332254-T-C

31187992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130332226-T-A

31187992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130332226-T-C

31187992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130332226-T-G

31188220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130332021-C-T

31188225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130332016-T-G

http://identifiers.org/hco/1/GRCh38#31188246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130331999-C-A

31188246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130331999-C-T

31188247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130331998-C-T

31188290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130331974-T-C

31188326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130331939-A-G

http://identifiers.org/hco/1/GRCh38#31188327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130331938-C-A

31188334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130331931-G-T

http://identifiers.org/hco/1/GRCh38#31188417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130331843-C-A

31188447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130331821-T-C

31190328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130331344-C-T

31190329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130331343-G-A

31190476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130331185-C-T

31190559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130331096-G-A

31190680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130330978-G-C

31190715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130330957-A-T

31198611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130327480-T-C

31198957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130327156-G-A

31199046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130327077-C-G

31199116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130327010-G-A

31199151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130326977-C-T

31199200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130326942-C-T

31199642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130326542-G-A

http://identifiers.org/hco/1/GRCh38#31199817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130326393-C-A

31199817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130326393-C-T

http://identifiers.org/hco/1/GRCh38#31201727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130324457-C-A

31201727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130324457-C-T

31201728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130324456-G-A

31201748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130324445-C-T

31201795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130324405-T-A

31201803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130324397-G-C

31201962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130324258-C-T

31202366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130323862-G-A

31204330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130321600-G-C

http://identifiers.org/hco/1/GRCh38#31204426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130321501-A-C

31204473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130321461-G-A

31204515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130321420-C-G

31204586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130321364-G-A

31204827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130321133-G-A

31204841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130321118-G-A

31204841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130321118-G-C

31204841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130321118-G-T

31214614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130319127-T-C

31214775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130319021-T-G

31214958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130318883-A-G

31215499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130318453-G-T

31215593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130318371-T-C

31215877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130318097-A-G

31216007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130317948-C-T

31216022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130317934-C-T

31216219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130317554-G-A

31216233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130317540-C-G

31216233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130317540-C-T

31216234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130317539-G-A

31216331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130317454-A-G

31216427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130317363-G-C

31218646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130314907-T-C

31218935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130314624-G-A

31219243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130314167-G-T

31219344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130314081-C-T

31219617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130313979-C-T

31219665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130313933-C-T

31221984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130312197-T-G

31222281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130311916-C-G

31222458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130311691-T-C

31222458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130311691-T-G

31222461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130311688-C-T

31222841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130311253-C-T

31222947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130311150-T-G

31223143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130311004-G-A

31223265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130310940-G-A

31223265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130310940-G-T

31223421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130310797-G-T

31223464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130310744-G-A

31223464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130310744-G-C

31223478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130310733-T-G

31223733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130310539-C-T

31223969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130310320-G-A

31224066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130310213-T-C

31224350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130309964-C-T

31224356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130309958-A-T

31225038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: -T-A

31225038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: -T-C

31227386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130307792-G-T

31227739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130307528-T-A

31227739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130307528-T-C

31228150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron_variant, undefined
orthologous variants: 130307127-C-T

31228379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130306933-G-C

31228593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130306740-T-C

31228619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130306714-G-A

31228864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130306475-G-C

31229016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130306286-C-G

31233709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130303459-G-A

31233736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130303440-T-C

http://identifiers.org/hco/1/GRCh38#31233773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130303405-C-A

31233773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130303405-C-T

31234255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130303105-C-G

31234828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130302590-G-A

31234869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130302556-C-T

31235233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130302190-G-C

31236295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130300508-C-T

31236466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130300344-T-C

31238109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130298743-T-C

31238215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130298658-G-T

31238452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130298452-G-C

http://identifiers.org/hco/1/GRCh38#31239150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130297799-A-C

http://identifiers.org/hco/1/GRCh38#31239451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130297569-C-A

31239451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: intron variant
orthologous variants: 130297569-C-T

http://identifiers.org/hco/1/GRCh38#31239606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130297481-C-A

31239606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: 130297481-C-T

http://identifiers.org/hco/1/GRCh38#31239658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#130297431-C-A

31239658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: 130297431-C-G

31239658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: 130297431-C-T

31239659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: 130297430-G-A

31239659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: 130297430-G-T

31239715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: 130297390-G-A

31239715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: 130297390-G-C

31239855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25743
most severe consequence: 5 prime UTR variant
orthologous variants: 130297264-A-G