101324538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3 prime UTR variant
orthologous variants: 56010084-G-T

101325612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3 prime UTR variant
orthologous variants: 56009029-A-T

101325768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3 prime UTR variant
orthologous variants: 56008885-T-C

101325904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3 prime UTR variant
orthologous variants: 56008769-A-T

http://identifiers.org/hco/3/GRCh38#101325919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56008754-C-A

101325919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3 prime UTR variant
orthologous variants: 56008754-C-G

101325919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3 prime UTR variant
orthologous variants: 56008754-C-T

101326090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56008586-G-A

101326090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56008586-G-T

101326093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56008582-A-G

101326103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56008572-G-A

101326103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56008572-G-T

http://identifiers.org/hco/3/GRCh38#101326119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56008556-C-A

101326119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56008556-C-T

101326641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56007346-G-C

101326708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56007267-G-A

101326725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56007250-A-G

101327461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56006684-T-A

101327551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56006648-T-G

101327647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56006585-T-G

101327778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense variant
orthologous variants: 56006458-T-C

101327778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense variant
orthologous variants: 56006458-T-G

http://identifiers.org/hco/3/GRCh38#101327953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56006283-C-A

101327953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56006283-C-T

101328229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56005769-T-C

101328325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56005684-G-A

http://identifiers.org/hco/3/GRCh38#101328433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56005234-A-C

101328733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56004466-G-A

101328733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56004466-G-T

101328776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56004424-T-G

http://identifiers.org/hco/3/GRCh38#101328808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56004392-C-A

101330287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56000988-A-T

101330325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56000948-C-T

101330622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56000673-A-G

101330855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56000445-T-C

101330879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56000421-G-C

http://identifiers.org/hco/3/GRCh38#101331083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56000224-A-C

101331840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56000126-A-T

http://identifiers.org/hco/3/GRCh38#101331841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56000125-A-C

101331905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56000063-C-T

101331954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56000014-T-A

101331971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 56000001-G-A

http://identifiers.org/hco/3/GRCh38#101332155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55999815-A-C

101332650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 55999509-A-G

101332650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 55999509-A-T

101332909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55999238-A-G

101332963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55999188-T-A

101332963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55999188-T-C

101332963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55999188-T-G

101332965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55999186-A-G

http://identifiers.org/hco/3/GRCh38#101332997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55999157-C-A

101333091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55999080-T-C

http://identifiers.org/hco/3/GRCh38#101333121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55999050-C-A

101333152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55999019-T-C

101333588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55998905-G-A

http://identifiers.org/hco/3/GRCh38#101336872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55996959-A-C

101336920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 55996914-T-C

101337044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 55996840-G-C

101337044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 55996840-G-T

101337109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 55996776-G-A

101337120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 55996766-G-A

101337120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron variant
orthologous variants: 55996766-G-T

101337196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55996700-G-T

101337208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55996688-T-C

101337317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55996628-G-T

101337321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55996624-G-A

101337321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55996624-G-T

101337397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55996552-A-T

101337431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55996528-A-G

http://identifiers.org/hco/3/GRCh38#101337761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55996031-C-A

101337877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55995916-A-G

101338328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55995792-T-C

http://identifiers.org/hco/3/GRCh38#101338804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55995327-A-C

101338898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55995198-T-G

101339056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55995027-A-G

101339129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55994971-G-T

101339226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55994874-T-C

101339312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55994494-T-C

101339312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55994494-T-G

101340004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55993814-G-T

101340048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55993680-T-A

101340048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55993680-T-C

101340062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55993666-A-G

101340243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55993457-G-A

101340243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55993457-G-T

101340338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55993338-T-C

101340578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55993210-T-C

101340615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55993168-A-G

101340668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55993125-T-G

101340773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55993047-A-G

http://identifiers.org/hco/3/GRCh38#101340824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55992993-A-C

101340939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55992881-G-A

101340951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55992868-G-A

101340951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55992868-G-C

101340954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55992865-A-G

101341074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55992760-G-A

101341088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55992746-T-C

http://identifiers.org/hco/3/GRCh38#101341532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55992339-C-A

http://identifiers.org/hco/3/GRCh38#101341560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55992311-C-A

101341568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55992303-A-T

101341742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55992148-A-G

http://identifiers.org/hco/3/GRCh38#101341798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55992101-A-C

101341798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55992101-A-G

http://identifiers.org/hco/3/GRCh38#101341807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55992092-C-A

101341879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55992002-C-T

http://identifiers.org/hco/3/GRCh38#101341887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55991990-A-C

101341895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991982-T-A

101341895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991982-T-C

101341895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991982-T-G

101341905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991972-G-C

101341905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991972-G-T

http://identifiers.org/hco/3/GRCh38#101341922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55991953-A-C

101341922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991953-A-T

http://identifiers.org/hco/3/GRCh38#101341926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55991949-A-C

101341961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991917-T-A

101342038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991843-T-C

101342166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991725-T-C

101342177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991721-T-A

http://identifiers.org/hco/3/GRCh38#101342206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55991703-C-A

http://identifiers.org/hco/3/GRCh38#101342735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55991263-C-A

101342735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991263-C-T

101342746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991252-A-G

101342827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55991181-A-G

101342993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990950-T-C

101342993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990950-T-G

101343021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990911-A-T

101343104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990839-G-A

101343133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990823-T-C

101343205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990749-C-T

101343237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990717-C-G

101343377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990580-T-C

101343546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990424-G-T

http://identifiers.org/hco/3/GRCh38#101343585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55990400-C-A

101343585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990400-C-T

101343599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990389-G-T

http://identifiers.org/hco/3/GRCh38#101343961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55990049-A-C

101344007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55990012-A-G

101344097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55989924-T-C

101344112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55989909-C-T

101344206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55989812-C-G

101344310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55989694-T-C

101344320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55989684-A-G

101344354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55989656-A-G

101344462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55989538-A-G

http://identifiers.org/hco/3/GRCh38#101344619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55989394-A-C

101344707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55989305-G-A

101344711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55989301-C-T

http://identifiers.org/hco/3/GRCh38#101347196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55986722-C-A

101347196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55986722-C-T

http://identifiers.org/hco/3/GRCh38#101347790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55986458-C-A

101347790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55986458-C-T

101347851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55986395-T-C

101347851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55986395-T-G

101348011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55986234-A-T

101348015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55986230-G-A

101348015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55986230-G-C

101348015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55986230-G-T

101348042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55986203-T-G

101348141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55986121-T-A

101348141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55986121-T-C

101350886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55983468-G-A

101350918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55983436-T-C

101351200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55983187-A-T

101351388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55983049-T-C

101351474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982969-A-G

101351515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982934-T-C

101351536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982914-A-G

101351549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982897-T-C

101351554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982892-T-C

http://identifiers.org/hco/3/GRCh38#101351591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55982796-C-A

101351591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982796-C-T

101351609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982778-A-G

101351665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982724-T-A

101351665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982724-T-C

101351684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982705-T-C

http://identifiers.org/hco/3/GRCh38#101351687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55982702-C-A

101351687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982702-C-T

101351733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982523-T-A

101351733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982523-T-C

101351734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982522-A-T

101351793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982405-A-G

101351795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982403-T-C

101351795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982403-T-G

http://identifiers.org/hco/3/GRCh38#101351799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55982399-C-A

101351799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982399-C-G

101351799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982399-C-T

101351925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982102-A-G

101351954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55982074-G-T

101351963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55982065-C-T

101352011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55982025-A-T

101352424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55981729-T-C

101352579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55981601-T-C

101353189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55981028-T-C

101353341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55980870-T-C

101353553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55980695-A-G

101353580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55980670-C-T

http://identifiers.org/hco/3/GRCh38#101353604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55980650-C-A

101353658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55980595-A-T

101353677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55980571-C-T

http://identifiers.org/hco/3/GRCh38#101353717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55980529-A-C

http://identifiers.org/hco/3/GRCh38#101359626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55979868-A-C

http://identifiers.org/hco/3/GRCh38#101359627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55979867-A-C

101361761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55978929-G-A

101361761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55978929-G-T

101361785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55978905-A-G

101361827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55978863-A-G

101361843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55978847-G-A

101361843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55978847-G-T

101361971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55978736-A-G

http://identifiers.org/hco/3/GRCh38#101361983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55978724-C-A

101361983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55978724-C-T

http://identifiers.org/hco/3/GRCh38#101364572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55976156-C-A

101364696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55976096-T-A

101364696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55976096-T-C

101364710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55976082-G-T

101364712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55976080-A-T

101364720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55976072-A-T

101365009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55975573-A-G

101365978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55974693-G-C

101366323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55974164-T-C

101366337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55974151-T-C

http://identifiers.org/hco/3/GRCh38#101366351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55974137-A-C

http://identifiers.org/hco/3/GRCh38#101366406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55974091-C-A

101366514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55973988-C-T

101366685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55973820-C-T

101366720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55973785-C-T

101366722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55973783-T-C

http://identifiers.org/hco/3/GRCh38#101366736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#55973769-C-A

101366737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55973768-A-T

101366830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55973677-T-C

101366921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55973589-T-C

101367191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55973217-C-G

101367440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55972458-T-C

101367591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55972366-T-G

101367786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971863-T-C

101367799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971850-T-C

101368025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971615-T-C

101368056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971586-G-A

101368056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971586-G-C

101368056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971586-G-T

101368123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971527-A-G

101368123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971527-A-T

101368149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971516-C-G

101368149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971516-C-T

101368214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55971461-C-T

101368866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55968956-G-T

101368921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55968898-T-C

101369024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55968799-T-C

http://identifiers.org/hco/3/GRCh38#101369368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55968425-C-A

101369368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55968425-C-T

101369454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55968330-G-A

101369519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55968250-C-G

101369570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55968178-A-G

http://identifiers.org/hco/3/GRCh38#101369629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55968029-C-A

http://identifiers.org/hco/3/GRCh38#101369960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55967568-A-C

101371445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55960222-C-G

101371472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55960192-T-C

101371814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55959636-G-T

http://identifiers.org/hco/3/GRCh38#101371880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55959573-C-A

101371932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55959525-T-C

http://identifiers.org/hco/3/GRCh38#101372065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#55959404-C-A

101372065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55959404-C-T

101372121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55959351-G-A

101372121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 55959351-G-T

http://identifiers.org/hco/3/GRCh38#101372174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55959105-A-C

101372174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55959105-A-G

101372174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55959105-A-T

101372183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55959096-G-T

101372257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55959018-G-A

101372257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55959018-G-T

101372348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55958952-T-A

101372348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55958952-T-C

101372375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55958935-A-G

101372510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55958819-A-G

101373302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55956244-A-G

101373316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55956232-T-C

101373337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55956211-T-A

101395710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953001-T-C

101395932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952806-G-A

101396298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952483-A-G

101396385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952398-G-A

101397778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55950650-A-T

101398010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55948229-T-C

101398124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55948150-G-A

101398988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55944207-G-T

101399103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944072-A-T

http://identifiers.org/hco/3/GRCh38#101399163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55944010-C-A

101399163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944010-C-T

http://identifiers.org/hco/3/GRCh38#101399168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55944005-C-A

101399168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944005-C-G

101399168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944005-C-T

101399323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943850-G-C

http://identifiers.org/hco/3/GRCh38#101399624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55943555-A-C

101399624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943555-A-G

101399641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943538-G-T

101417331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55932394-T-C

101417331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55932394-T-G

101417903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55931846-T-A

101417903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55931846-T-C

101417903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55931846-T-G

http://identifiers.org/hco/3/GRCh38#101417937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55931814-A-C

101418096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55931662-A-G

http://identifiers.org/hco/3/GRCh38#101418116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55931642-A-C

101418799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55930523-A-G

101418937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55930392-A-G

101418996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55930332-T-C

101458277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55918706-G-A

101458477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55918507-A-G

http://identifiers.org/hco/3/GRCh38#101458496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55918485-C-A

101458496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55918485-C-T

http://identifiers.org/hco/3/GRCh38#101458707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55918031-C-A

101458707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55918031-C-T

http://identifiers.org/hco/3/GRCh38#101458797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55917946-C-A

101458834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917918-G-A

101458834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917918-G-C

101458834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917918-G-T

101458883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917873-A-G

http://identifiers.org/hco/3/GRCh38#101458906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55917850-C-A

101458928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917821-A-G

101458965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55917782-A-G

101459000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55917753-T-G

101459094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917667-T-A

101459094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917667-T-C

http://identifiers.org/hco/3/GRCh38#101459106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55917655-C-A

101459106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917655-C-T

101493558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55910114-C-T

101493561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55910111-G-A

http://identifiers.org/hco/3/GRCh38#101493564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55910108-C-A

http://identifiers.org/hco/3/GRCh38#101493728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55909953-C-A

101493728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55909953-C-T

101493857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55909833-T-C

101494281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55909454-T-C

101494289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55909446-A-G

101500080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55904170-T-C

101500208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55903922-T-G

101500971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902854-A-G

101500971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902854-A-T

101500986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902843-A-G

101500986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902843-A-T

101500996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902833-A-G

http://identifiers.org/hco/3/GRCh38#101501001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55902829-C-A

101501001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902829-C-G

101501014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902816-A-G

101501016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902814-T-C

101501022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902808-T-A

101501022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902808-T-C

101501022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902808-T-G

http://identifiers.org/hco/3/GRCh38#101501023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55902807-A-C

101501024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902806-T-A

101501024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902806-T-G

101501039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902791-A-G

101501064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902775-G-T

101501182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902658-A-G

101501531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902385-T-C

101501585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902291-A-G

101501611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55902268-C-T

101511145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55898182-T-A

101511231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55897813-C-T

101511335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55897715-T-C

101511590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55897473-T-A

101511951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896983-C-T

101512278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55896738-C-T

http://identifiers.org/hco/3/GRCh38#101512556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55896475-C-A

101512581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896452-G-A

101512760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55896276-G-T

101512801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896232-G-C

http://identifiers.org/hco/3/GRCh38#101512921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#55896113-A-C

101512951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896103-T-G

http://identifiers.org/hco/3/GRCh38#101512952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#55896102-C-A

101512958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896096-T-G

101512961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896093-G-A

101512961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896093-G-T

101513043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55895985-C-T