7797460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195073-C-G

7797520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195126-T-G

7797525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195131-G-A

7797525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195131-G-T

7797653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195233-T-C

7797748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195307-G-C

7797748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195307-G-T

7797871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195416-T-C

http://identifiers.org/hco/9/GRCh38#7797991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75195499-C-A

7797991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195499-C-T

7798001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195509-T-G

7798055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195529-C-T

7798089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3 prime UTR variant
orthologous variants: 75195563-T-A

http://identifiers.org/hco/9/GRCh38#7798252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75195657-A-C

7798252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75195657-A-G

http://identifiers.org/hco/9/GRCh38#7798253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75195658-C-A

7798254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75195659-A-G

7798264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75195664-G-A

7798356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75195729-A-T

7798369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75195742-T-C

7798370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75195743-T-A

7798370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75195743-T-C

http://identifiers.org/hco/9/GRCh38#7798371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75195744-C-A

7798371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75195744-C-T

7798429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75195803-T-C

http://identifiers.org/hco/9/GRCh38#7798437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: http://identifiers.org/mco/4/GRCm39#75195811-C-A

7798437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 75195811-C-G

7798437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_retained_variant
orthologous variants: 75195811-C-T

7798439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195813-G-T

7798470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195846-C-G

7798515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195888-G-T

7798522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195895-G-C

7798522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195895-G-T

7798528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195901-C-G

7798528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195901-C-T

7798536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195909-G-A

7798536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195909-G-C

7798536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75195909-G-T

7798669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196044-T-A

7798669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196044-T-C

7798722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196095-T-C

http://identifiers.org/hco/9/GRCh38#7799418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196167-C-A

7799418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196167-C-G

7799418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196167-C-T

7799423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196172-A-G

7799432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196181-C-T

7799470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75196227-T-C

http://identifiers.org/hco/9/GRCh38#7799495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196252-A-C

7799495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75196252-A-G

http://identifiers.org/hco/9/GRCh38#7799542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196299-C-A

7799542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75196299-C-G

7799542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75196299-C-T

http://identifiers.org/hco/9/GRCh38#7799558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196315-C-A

7799558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75196315-C-G

http://identifiers.org/hco/9/GRCh38#7799647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196404-C-A

7799686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75196440-G-A

http://identifiers.org/hco/9/GRCh38#7799692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196446-C-A

http://identifiers.org/hco/9/GRCh38#7799723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196477-C-A

7799723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75196477-C-G

7799723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75196477-C-T

http://identifiers.org/hco/9/GRCh38#7799820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196555-A-C

7799860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196577-G-A

7799860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196577-G-T

7799889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196599-T-C

7799959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196651-T-A

7799959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196651-T-C

7799959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196651-T-G

7799962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196654-G-A

7799962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196654-G-C

7799962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196654-G-T

7799975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196670-T-A

7799975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196670-T-C

7799975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196670-T-G

http://identifiers.org/hco/9/GRCh38#7799984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196679-C-A

7799984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196679-C-G

7799984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196679-C-T

http://identifiers.org/hco/9/GRCh38#7800005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196684-C-A

http://identifiers.org/hco/9/GRCh38#7800008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196687-C-A

http://identifiers.org/hco/9/GRCh38#7800010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196689-C-A

7800010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196689-C-T

7800036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196714-C-G

7800036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196714-C-T

http://identifiers.org/hco/9/GRCh38#7800052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75196729-C-A

7800052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75196729-C-T

7803088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197067-T-C

7803108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197079-G-C

7803108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197079-G-T

7803218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197525-G-T

7803379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198106-T-C

7803382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198109-G-A

7803493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198223-G-A

7803501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198231-A-G

7803507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198234-G-T

7803526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198253-A-G

7803592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198293-C-T

http://identifiers.org/hco/9/GRCh38#7803835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75198498-C-A

7803898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198561-A-G

7804078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198725-T-A

7804080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198730-A-G

7804158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198782-T-C

7804182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198801-C-G

7804621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200082-A-G

7804692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200153-A-G

7804696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200157-C-T

7804793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200261-A-G

7804896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200362-C-T

7804948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200419-C-T

7804949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200420-T-C

7805034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200505-T-C

7805034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200505-T-G

7805072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200544-T-C

7805266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200716-G-A

7805399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200820-C-T

7805454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200863-A-T

7805634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200960-A-G

7805650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200976-C-T

7805665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200990-G-A

7805665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200990-G-T

7805817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201241-C-G

7805939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201365-G-A

7805939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201365-G-T

7805984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201405-T-G

7806698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201884-G-A

7806698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201884-G-C

7806702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201887-C-T

7806739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201927-A-T

7806740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201928-T-C

7806798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75201992-A-G

7806908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75202065-A-G

http://identifiers.org/hco/9/GRCh38#7806944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75202101-C-A

7806993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75202160-G-A

7807047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75202208-G-A

7807051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75202212-G-A

7809395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75204889-A-G

7809495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75204968-T-G

7809533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75205005-C-G

7809533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75205005-C-T

7809536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75205008-T-C

7809536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75205008-T-G

7811339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75207603-A-T

7811399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75207661-T-A

7811513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75207771-A-G

7811590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75207861-G-C

7811982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75208247-G-A

7812034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75208305-A-G

7812415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75209843-A-G

7812428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75209856-C-T

7812709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210092-T-C

7812799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210176-C-T

7812966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210353-A-G

7813063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210450-G-T

7813109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210496-G-A

7813318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210707-G-A

7813529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210920-A-G

7813578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210968-A-G

7813688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75211054-C-G

7813876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75211255-A-G

7814025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75211405-A-G

7814185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75211548-T-C

7814188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75211551-A-G

http://identifiers.org/hco/9/GRCh38#7814305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75211690-A-C

7814418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75211801-A-G

7814871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212095-C-T

7814991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212203-T-C

7815161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212358-G-T

7815184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212381-A-G

7815202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212399-A-G

7816026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75213069-C-G

7816305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75213278-C-T

7816557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75213481-A-T

7816565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75213489-T-C

7816702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75213633-A-G

7817883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75213947-A-G

http://identifiers.org/hco/9/GRCh38#7817922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75213986-A-C

7827247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75218712-C-T

7827351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75218621-T-A

7827351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75218621-T-G

7827365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75218607-G-A

7827365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75218607-G-C

7827365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75218607-G-T

http://identifiers.org/hco/9/GRCh38#7827408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75218583-C-A

7827626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75218320-G-T

7827697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75218265-T-C

7829513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229123-T-A

7829520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229130-C-T

7829620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229206-T-A

7833976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: non coding transcript exon variant
orthologous variants: 75229462-G-T

http://identifiers.org/hco/9/GRCh38#7833995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75229477-C-A

7833995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: non coding transcript exon variant
orthologous variants: 75229477-C-T

7834036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229519-G-A

7834046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229529-C-G

7834130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229613-C-G

7834130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229613-C-T

7834150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229633-A-G

7834321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229795-C-T

http://identifiers.org/hco/9/GRCh38#7834322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75229796-A-C

7834404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229897-A-G

http://identifiers.org/hco/9/GRCh38#7834463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75229956-C-A

7834463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229956-C-T

7834512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229990-C-T

7834620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75230111-C-T

http://identifiers.org/hco/9/GRCh38#7834778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75233788-A-C

7834793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233803-A-G

7834911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233917-A-G

7834911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233917-A-T

7834982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75235834-C-T

http://identifiers.org/hco/9/GRCh38#7835044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75235908-A-C

7837754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238441-C-T

7837836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238521-T-C

7837974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238711-G-C

7837974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238711-G-T

7838070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238803-G-C

7838073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238806-G-A

7838923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75239786-C-T

7840790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75246914-A-T

7840976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247100-A-G

7841341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247143-A-G

http://identifiers.org/hco/9/GRCh38#7841726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75247515-C-A

7841907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247675-G-A

7841962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247713-T-C

7842045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247772-C-G

7842214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247939-G-C

7842438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248167-T-A

7842520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248248-A-G

7842690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248422-T-C

7842695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248427-A-G

7842886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248609-G-A

7842886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248609-G-T

7842908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248631-A-T

http://identifiers.org/hco/9/GRCh38#7843053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75248754-A-C

7843085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248786-T-C

7843614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75253186-A-G

7843958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75253519-G-A

7844011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75253558-T-G

7844128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75253661-T-C

7844214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75253761-T-A

7844223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75253770-G-A

7844364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75253917-C-T

7844567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75254112-T-A

7844567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75254112-T-C

7844567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75254112-T-G

http://identifiers.org/hco/9/GRCh38#7844806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75254318-C-A

7845375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75254672-C-T

7845565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75254847-G-C

7845573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75254855-G-A

7845596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75254878-C-T

http://identifiers.org/hco/9/GRCh38#7846141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75256685-C-A

7846141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75256685-C-G

7846153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75256697-A-G

7846173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75256711-T-G

http://identifiers.org/hco/9/GRCh38#7854393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75258620-A-C

7856818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75264705-G-C

7856820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75264707-C-G

7856873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75264760-C-G

7857161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75266815-G-A

7857237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75266877-A-G

7857639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75274467-G-A

7857657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75274483-A-T

7857784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75274607-C-G

http://identifiers.org/hco/9/GRCh38#7857832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75274646-C-A

http://identifiers.org/hco/9/GRCh38#7857975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75274786-A-C

7858087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75274903-A-T

7858133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276223-A-T

7858148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276238-T-A

7858224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276694-C-G

7858261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276731-T-C

7858268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276741-T-C

7858310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276785-A-G

7858323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276798-G-A

http://identifiers.org/hco/9/GRCh38#7858440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75276914-C-A

7858440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276914-C-T

http://identifiers.org/hco/9/GRCh38#7858459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75276933-C-A

7858466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276940-C-T

7858740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277200-T-G

7858795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277258-G-A

7858821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277298-A-G

7858947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277398-C-T

7858978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277429-G-A

7858978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277429-G-C

7858978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277429-G-T

7858989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277440-A-G

7858995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277446-A-G

7859316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277728-G-C

7859332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277744-T-C

7859440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75277849-A-G

7859995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278362-G-A

7860126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278486-G-C

7860126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278486-G-T

7860280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278630-G-A

7860283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278633-C-G

7860322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278672-T-G

7860629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278928-T-G

7860651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278959-A-G

7872885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300896-G-T

7872900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300914-T-C

7872902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300916-C-G

7872955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300981-G-C

7873066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75301068-C-T

7873490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75301478-C-G

7873694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75301710-C-T

7874351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75302019-A-G

7874362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75302030-G-C

7874498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304037-C-G

7874500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304039-G-T

7874522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304055-C-T

7874596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304124-T-C

7874632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304160-T-C

7874658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304191-C-T

7874659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304192-G-A

7874845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304370-C-G

7874959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304476-C-T

7875352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304866-A-G

7875355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304869-G-A

7875355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304869-G-T

7875534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75305042-A-G

7875534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75305042-A-T

7875540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75305048-C-T

7875544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75305052-G-C

7878075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75305178-G-A

7878076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75305179-C-G

7878265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75305399-C-T

7878538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75305637-A-G

7878734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75305850-T-C

http://identifiers.org/hco/9/GRCh38#7878923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#75306023-C-A

7879037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75306133-A-G

7879209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30536
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75307782-C-G