105235298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 83484053-G-A

105235322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 83484077-G-A

105235409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484146-G-C

105235423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484160-G-A

105235733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484325-C-T

105235814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484344-G-A

105235814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484344-G-C

105235814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484344-G-T

105235824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484351-G-A

105235824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484351-G-T

http://identifiers.org/hco/12/GRCh38#105235911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#83484372-C-A

105235911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484372-C-T

105235953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484386-A-G

105235953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484386-A-T

105235954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484387-G-A

105235954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484387-G-C

105235954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484387-G-T

105235968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 83484401-G-A

105235968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484401-G-T

105235992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 83484425-G-A

105235992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 83484425-G-T

105236038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484471-T-C

http://identifiers.org/hco/12/GRCh38#105236051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#83484472-C-A

105236051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484472-C-T

105236088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484499-G-A

105236088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484499-G-C

105236088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484499-G-T

105236089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484500-G-A

105236089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484500-G-C

105236089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484500-G-T

http://identifiers.org/hco/12/GRCh38#105236197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#83484569-C-A

105236197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484569-C-T

105236252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484612-G-A

105236252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484612-G-T

105236262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484622-C-G

105236262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484622-C-T

http://identifiers.org/hco/12/GRCh38#105236313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#83484688-C-A

105236335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484721-G-A

105236335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484721-G-T

105236344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484730-G-A

105236349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484736-T-G

105236350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83484737-G-T

105237544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487082-C-G

105237547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487085-A-G

105237640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487148-G-A

http://identifiers.org/hco/12/GRCh38#105237852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83487360-C-A

105237852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487360-C-G

105237968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487477-T-G

105237993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487502-G-A

105238030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487534-A-T

105238159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487655-A-G

105238159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487655-A-T

105238369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487805-A-G

105238411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487837-C-T

105238547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83487961-C-T

105252686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83494798-G-A

105253005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497099-T-G

105253026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497120-G-C

105253026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497120-G-T

105253097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497190-C-T

105253113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497206-T-C

105253113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497206-T-G

105253155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497245-A-G

105253220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497309-A-G

105253375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497425-T-A

105253404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497443-C-T

105253409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497448-A-G

105253643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497601-C-G

105253702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497671-T-A

105253703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497672-C-T

105253789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497797-C-T

105253867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497887-C-T

105253883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497903-T-A

105253926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497916-G-A

http://identifiers.org/hco/12/GRCh38#105254057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83498007-C-A

105254165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83498084-C-T

http://identifiers.org/hco/12/GRCh38#105254227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83498129-C-A

105254229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83498131-G-A

105254314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83498192-G-T

105257044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83500073-C-T

105257142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83500156-T-C

105257397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83500366-A-T

105257560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83500521-C-T

105257717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83500696-A-G

105257776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83500755-G-A

105257820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83500790-G-A

105258240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83501585-A-T

105258533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83502228-G-A

105258710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83502395-A-G

105258710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83502395-A-T

http://identifiers.org/hco/12/GRCh38#105258725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83502407-C-A

105258853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83502481-C-T

105259167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83502752-C-T

105259216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83502801-G-T

105259438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83503414-G-T

105259596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83503551-T-G

105259892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83503877-A-G

105259892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83503877-A-T

105260704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83513897-C-T

105260811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83514004-A-T

105261120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83516098-T-G

105261216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83516174-G-A

http://identifiers.org/hco/12/GRCh38#105261290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83516222-C-A

105261293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83516225-C-G

http://identifiers.org/hco/12/GRCh38#105261352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83516264-A-C

105261352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83516264-A-T

105261370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83516282-C-T

105261555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83516426-G-T

105261558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83516429-T-G

105262850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83517312-T-C

105262943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83517386-T-C

105263045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83517471-G-A

105263093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83517497-T-G

http://identifiers.org/hco/12/GRCh38#105263187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83517588-C-A

105263187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83517588-C-T

105268287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83521170-G-A

105268287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83521170-G-T

105268638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83522282-C-T

105268640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83522284-A-G

105268671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83522317-C-T

105268899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83522555-C-G

105269122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83523472-A-G

105269185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83523534-T-C

105271726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83524904-A-T

105271868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83525536-G-T

105276909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83525946-C-T

http://identifiers.org/hco/12/GRCh38#105276949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83525977-C-A

105280461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83526675-C-T

105280464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83526678-C-T

http://identifiers.org/hco/12/GRCh38#105280835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83527019-C-A

105280901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527196-C-G

105280901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527196-C-T

105280909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527227-C-T

105280910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527228-A-G

http://identifiers.org/hco/12/GRCh38#105280916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83527253-A-C

105280916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527253-A-G

105280962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527299-T-C

105281045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527380-G-C

105281263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527785-T-C

105281440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527952-G-A

105281440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527952-G-C

105281502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83527971-C-T

105281829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83528181-T-C

http://identifiers.org/hco/12/GRCh38#105281967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83528286-A-C

105282005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83528326-G-A

105282017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83528338-T-G

105282086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83528404-A-T

105285503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83533303-T-A

105285684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83533484-C-T

105285837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83533667-A-G

105285904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83533708-T-C

http://identifiers.org/hco/12/GRCh38#105286120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83533963-C-A

105286144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83533987-T-C

http://identifiers.org/hco/12/GRCh38#105286862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83534069-A-C

105287320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83534886-T-C

105287416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83534977-T-G

105287489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83535055-C-T

105287795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83535348-G-A

105287809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83535362-A-G

105288341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83535766-T-C

105288436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83535858-A-G

105288693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83536095-A-G

http://identifiers.org/hco/12/GRCh38#105288703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83536105-C-A

105289124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83537600-C-T

105289146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83537621-T-C

105289522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83537998-G-A

http://identifiers.org/hco/12/GRCh38#105290291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83538858-C-A

105290560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83539276-T-C

105290706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83539475-G-C

105290710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83539479-G-T

105290736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83539505-C-T

105290737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83539506-A-G

http://identifiers.org/hco/12/GRCh38#105293149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83541047-C-A

105293149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83541047-C-G

http://identifiers.org/hco/12/GRCh38#105293331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83541247-A-C

105293423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83541324-C-T

105293463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83541366-A-G

105295506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83542331-C-G

http://identifiers.org/hco/12/GRCh38#105295552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83542375-C-A

105295806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83542627-T-C

105295875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83542693-G-T

105296047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83542851-C-T

105296084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83542878-G-A

105296090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83542884-T-G

http://identifiers.org/hco/12/GRCh38#105296091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83542885-C-A

105296091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83542885-C-T

105298117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83543521-A-G

105315151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83544390-G-C

105315152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83544392-A-G

105315602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83544839-G-A

105315768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83545818-C-T

105316038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83546071-C-T

105316071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83546104-G-A

105316296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83546296-A-G

105316306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83546306-T-G

105316315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83546315-T-C

105316383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83546381-T-C

105317404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83546943-C-T

105317772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83547588-A-G

105317800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83547613-A-G

105317843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83547656-A-G

105317880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83547694-T-A

105317938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83547752-A-T

http://identifiers.org/hco/12/GRCh38#105326806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83554695-C-A

105326812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83554701-G-A

105326826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83554715-C-T

105326847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83554734-C-T

http://identifiers.org/hco/12/GRCh38#105326900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#83554774-C-A

105326900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83554774-C-T

105327044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: non coding transcript exon variant
orthologous variants: 83554913-T-C

105327064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 83554933-G-A

105327115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83554985-G-A

105327115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83554985-G-T

105327266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83555083-T-C

105327470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83555265-A-T

105328064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83555460-T-C

105328079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83555470-G-A

105328398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83555787-C-T

105328712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83556090-C-T

105328847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83556204-T-C

105328877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83556235-C-T

105329863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83558062-C-T

105330125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83558225-C-T

105330207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83558305-A-G

105330473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83558575-G-A

105330973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83558935-G-A

105330973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83558935-G-C

105330973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83558935-G-T

105331015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83558964-T-C

105331098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83559041-C-T

105331382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83559263-G-C

105331383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83559264-T-G

105331469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83559337-T-C

105331524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83559394-G-A

http://identifiers.org/hco/12/GRCh38#105331861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83559691-A-C

105331937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83559767-C-G

105331944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83559774-A-G

105332062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83560320-A-G

105332262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83560503-G-A

http://identifiers.org/hco/12/GRCh38#105332536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83561009-A-C

105332536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83561009-A-G

http://identifiers.org/hco/12/GRCh38#105332860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83561915-A-C

105332860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83561915-A-T

105333160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83562211-T-C

105333319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83562371-C-T

105333353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83562402-T-G

http://identifiers.org/hco/12/GRCh38#105333359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83562408-A-C

105333363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83562412-G-C

105333378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83562427-T-C

105333410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83562450-C-T

http://identifiers.org/hco/12/GRCh38#105333514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83562572-C-A

105333543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83562595-A-G

105334104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83563255-G-A

105334221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83563334-C-T

105334242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83563354-G-T

105334431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83563526-C-T

105334439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83563537-A-G

105334934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83565745-T-C

http://identifiers.org/hco/12/GRCh38#105335071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83565868-A-C

105335338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83566122-G-A

105335426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83566196-T-C

105335450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83566236-C-T

105335453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83566239-T-A

105335804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83567133-C-T

105335936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83567251-G-C

105336010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83567326-T-C

105336245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83567618-C-T

105336317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83567677-T-C

105336400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83567758-G-T

105336438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83567796-T-C

105336522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83567858-C-T

105336524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83567860-G-C

105336666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83568015-C-T

105336704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83568048-A-G

105336795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83568139-G-A

105339239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83569352-A-T

105339246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83569359-T-C

105339275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83569387-T-C

105339988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83569951-C-T

105340025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83569988-A-G

105340025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83569988-A-T

105343661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83571957-C-T

http://identifiers.org/hco/12/GRCh38#105343770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83572076-C-A

105344085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83572438-G-T

105344115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83572468-G-A

105344152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83572506-G-A

105344293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83572662-C-T

http://identifiers.org/hco/12/GRCh38#105348497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83573676-C-A

105348497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83573676-C-T

105348505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83573684-T-C

105348592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83573763-T-C

105348700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83573868-T-C

105348824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83574001-A-G

105348959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83574117-C-T

105348970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83574128-G-A

105348970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83574128-G-C

105350041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83575573-C-T

105352145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83576488-G-C

105352252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83576565-T-A

105352262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83576575-G-C

105352773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83577255-C-T

http://identifiers.org/hco/12/GRCh38#105352801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83577275-A-C

105353241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83577684-G-A

105353241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83577684-G-T

105353252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83577690-T-C

105353321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83577754-A-G

http://identifiers.org/hco/12/GRCh38#105353393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83577820-C-A

105353456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83577862-G-A

105353522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83577922-G-A

105353522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83577922-G-T

105353562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83578074-G-A

105353562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83578074-G-C

http://identifiers.org/hco/12/GRCh38#105353574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83578097-A-C

105353867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83578566-G-T

105355158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83579986-A-T

http://identifiers.org/hco/12/GRCh38#105355831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83580291-A-C

105355864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83580313-G-C

105355899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83580344-G-A

http://identifiers.org/hco/12/GRCh38#105355966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83580408-C-A

105356007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83580465-C-T

105356132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83580573-T-C

105356375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581293-C-T

105356400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581308-T-C

105356425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581338-G-A

105356425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581338-G-C

105356425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581338-G-T

http://identifiers.org/hco/12/GRCh38#105356511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83581414-C-A

105356511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581414-C-T

105356566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581469-T-C

105356665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581551-A-G

105356714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581600-C-T

105356801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83581687-T-G

http://identifiers.org/hco/12/GRCh38#105356852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83581943-A-C

105356941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83582027-T-C

105357051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83582127-A-G

105357067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83582143-C-T

105357085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83582161-C-T

105357132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83582206-C-T

105357275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83582346-G-A

105357277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83582347-A-T

105357438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83582451-T-C

105358610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83582866-T-C

105358835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83583072-T-C

105358952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83583153-C-T

105359830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83586210-T-C

105359853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83586233-T-C

105359860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83586239-G-A

105359873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83586252-T-G

105359998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83586373-A-G

105360525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83586839-A-G

105361473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83587187-G-A

105361564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83588993-A-G

105363322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83590451-A-G

105364109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83591478-T-C

105364138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83591512-G-T

105364291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83591658-A-G

105364543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83591860-C-G

105364543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83591860-C-T

105364718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83592059-T-A

105364836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83592170-C-T

105365331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83592846-G-A

105365351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83592866-G-A

http://identifiers.org/hco/12/GRCh38#105365419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83592930-A-C

105365526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83593072-G-C

http://identifiers.org/hco/12/GRCh38#105365757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83593258-C-A

105366093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593520-G-A

105366093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593520-G-T

105366162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593587-T-C

http://identifiers.org/hco/12/GRCh38#105366178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83593609-C-A

105366178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593609-C-G

http://identifiers.org/hco/12/GRCh38#105366218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83593654-C-A

105366218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593654-C-T

http://identifiers.org/hco/12/GRCh38#105366413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83593832-A-C

105366413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593832-A-G

105366413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593832-A-T

105366416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593835-T-C

105366453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593862-A-G

http://identifiers.org/hco/12/GRCh38#105366459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83593868-C-A

105366459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593868-C-G

105366459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83593868-C-T

105366817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83594773-T-C

http://identifiers.org/hco/12/GRCh38#105366841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83594795-C-A

105366841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83594795-C-T

105367010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83594991-G-A

105367058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595032-C-G

105367428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595418-A-G

105367493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83595478-G-A

105367493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83595478-G-T

http://identifiers.org/hco/12/GRCh38#105367513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83595498-C-A

105367513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595498-C-G

105367513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595498-C-T

105367637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595602-C-G

105367642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595607-G-A

105367642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595607-G-T

105367651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595613-T-G

105367705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595643-T-A

http://identifiers.org/hco/12/GRCh38#105367775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83595716-A-C

105368259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595848-A-G

105368259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595848-A-T

105368304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595890-A-G

105368304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595890-A-T

105368337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595921-G-C

105368371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83595953-T-G

105368704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83596287-A-G

105368859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83596440-C-T

http://identifiers.org/hco/12/GRCh38#105368924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83596494-A-C

105369123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83596692-C-T

105369192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83596741-A-T

105369341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83596854-A-G

105369552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83596874-A-T

105370095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83597226-T-A

105370095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83597226-T-C

105370197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83597356-A-T

105370263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83597421-T-C

105370546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83597690-A-G

105370587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83597727-T-C

105370885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83597986-C-T

http://identifiers.org/hco/12/GRCh38#105370941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83598047-A-C

105370941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83598047-A-G

105371001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83598107-T-C

105371075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83598177-G-A

105371075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83598177-G-T

105371411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 83598516-A-G

105371567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron variant
orthologous variants: 83598679-G-A

105373524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83600912-C-T

105373597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83601018-T-A

105373601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83601022-G-T

105374124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83601905-C-T

105374140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83601921-A-G

105374156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83601939-A-G

105378551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83603443-G-A

105378656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83603545-A-T

105378673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83603562-T-G

http://identifiers.org/hco/12/GRCh38#105378689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83603577-C-A

105378689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83603577-C-G

105378689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83603577-C-T

105378765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83603579-T-A

105378765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83603579-T-C

105378765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83603579-T-G

105378766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83603580-A-G

105378792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83603606-G-A

105378792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83603606-G-T

105378826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83603693-G-A

105378826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83603693-G-T

105379046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83603976-C-T

105383201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83611859-G-A

105383215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83611873-G-A

http://identifiers.org/hco/12/GRCh38#105383709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83612633-C-A

105392497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83614599-T-C

105392507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83614609-A-G