100989661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115722702-G-T

100989663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115722699-C-T

100989844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115722569-T-C

100989853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115722560-A-G

100989872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115722553-G-T

100989884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115722543-G-A

100989922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115722511-A-G

100989922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115722511-A-T

100989928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115722505-G-A

100989928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115722505-G-T

100990339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115722436-G-C

100990339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115722436-G-T

100990529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 115722258-C-T

http://identifiers.org/hco/1/GRCh38#100990659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115722121-C-A

100990687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115722088-C-T

100990943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115721714-G-C

http://identifiers.org/hco/1/GRCh38#100990986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115721664-A-C

100991076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115721579-T-C

100992330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720734-T-C

100992538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720536-G-T

100992541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720534-T-A

100992576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720500-A-T

http://identifiers.org/hco/1/GRCh38#100992612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115720471-A-C

http://identifiers.org/hco/1/GRCh38#100992621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115720462-C-A

100992621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720462-C-T

100992687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115720397-T-C

http://identifiers.org/hco/1/GRCh38#100992775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115720310-C-A

100992806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720283-A-G

100992838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720249-G-T

http://identifiers.org/hco/1/GRCh38#100992873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115720219-C-A

100992873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720219-C-T

100992942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720148-T-G

http://identifiers.org/hco/1/GRCh38#100992956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115720134-C-A

100993067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115720021-C-T

100993212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115719841-G-A

http://identifiers.org/hco/1/GRCh38#100995020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115718982-C-A

http://identifiers.org/hco/1/GRCh38#100995023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115718979-C-A

http://identifiers.org/hco/1/GRCh38#100995038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115718965-C-A

100995038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718965-C-T

100995040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718963-T-C

100995048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718955-G-C

100995048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718955-G-T

100995053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718950-T-C

100995069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718934-G-T

http://identifiers.org/hco/1/GRCh38#100995158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115718850-A-C

100995158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718850-A-G

http://identifiers.org/hco/1/GRCh38#100995197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115718816-C-A

100995197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718816-C-T

100995250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718765-C-T

http://identifiers.org/hco/1/GRCh38#100995255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115718760-C-A

100995255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718760-C-T

100995353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718656-T-A

100995353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718656-T-C

100995388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718622-A-G

100995428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718586-T-C

100995457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115718558-G-T

100995556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115718456-T-C

http://identifiers.org/hco/1/GRCh38#100995557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115718455-C-A

100995565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115718447-T-C

http://identifiers.org/hco/1/GRCh38#100995689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115718361-C-A

100995784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115718272-T-C

100995784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115718272-T-G

http://identifiers.org/hco/1/GRCh38#100995822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115718235-C-A

100995901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115718166-G-T

100996085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115717984-T-C

100996889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115717487-T-C

101000809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115709363-G-C

101000837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115709335-T-C

101000837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115709335-T-G

http://identifiers.org/hco/1/GRCh38#101000857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115709322-C-A

101000907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115709274-A-G

101000968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115709216-G-A

101001009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115709185-T-A

101001061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115709134-T-C

101001067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115709126-T-A

101001249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115709015-T-C

101001330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708960-G-T

101001335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708955-G-A

101001335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708955-G-T

101001344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708946-G-A

101001344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708946-G-C

101001344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708946-G-T

101001359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708931-G-T

101001395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708891-T-A

101001395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708891-T-G

101001419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708855-G-T

101001433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708841-T-C

101001556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115708718-A-G

http://identifiers.org/hco/1/GRCh38#101001891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115708425-A-C

101002099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708203-G-C

101002133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708169-T-C

101002362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115701677-T-G

101002408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115701661-A-T

101002416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115701650-T-A

101002548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115701527-C-T

101002628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115701448-C-G

101002932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115701175-A-T

http://identifiers.org/hco/1/GRCh38#101003011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115699856-A-C

101003012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699855-T-C

101003073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699794-G-A

101003253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699650-C-T

101003383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699584-T-C

101003449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699529-A-G

101003454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699524-T-C

101003602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699391-G-C

101003602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699391-G-T

101003648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699344-A-G

101003723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115699282-C-T

101004065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115698982-A-G

101004065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115698982-A-T

http://identifiers.org/hco/1/GRCh38#101004253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#115698805-C-A

101004625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115698394-C-G

101004647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115698362-A-G

http://identifiers.org/hco/1/GRCh38#101004672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115698336-A-C

101004679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115698329-T-C

101004726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115698283-C-T

101004736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115698269-G-A

101004787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115698234-G-A

101004964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115698085-T-C

101005114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115697820-T-C

101005230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115697635-G-C

http://identifiers.org/hco/1/GRCh38#101006407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115696537-C-A

101006547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115696438-G-C

101006681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115696321-C-T

101006693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115696310-C-T

101006782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115696234-T-C

101006808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115696208-T-C

101010187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115696055-G-A

http://identifiers.org/hco/1/GRCh38#101010191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115696051-A-C

101010230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115696035-A-G

101010280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115696002-T-G

101010292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115695990-A-G

101010499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115695861-T-G

101010769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115695546-C-T

101010780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115695535-T-C

101010842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115695499-G-T

101012510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115694734-T-G

101012649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115694630-G-T

101012666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115694618-C-G

101012666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115694618-C-T

101012991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115694168-T-C

http://identifiers.org/hco/1/GRCh38#101013586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115693544-C-A

101013586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115693544-C-T

101013602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115693528-A-G

101013753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115693407-T-A

101013753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115693407-T-G

101013950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115693230-A-G

101013952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115693228-A-G

101013962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115693218-T-C

101017371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115692466-T-C

101018122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115691706-G-A

101018187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115691642-A-G

http://identifiers.org/hco/1/GRCh38#101018204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115691625-C-A

101018815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115691170-G-T

101019176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115690804-C-T

101019182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115690797-T-C

101019822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115690130-T-A

101019837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115690112-A-G

101020031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689891-G-A

101020031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689891-G-C

101020035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689886-A-G

101020042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689879-A-G

http://identifiers.org/hco/1/GRCh38#101020222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115689736-C-A

101020237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689721-C-T

101020447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689626-T-C

101020451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689622-C-T

101020474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689599-G-C

http://identifiers.org/hco/1/GRCh38#101020477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115689596-C-A

101020477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689596-C-G

101020552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689529-A-G

101020835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115689376-C-G

101020991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115687079-T-C

101021317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115686749-T-G

101021412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115686651-G-C

101021538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115686564-T-C

http://identifiers.org/hco/1/GRCh38#101021787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115686337-C-A

http://identifiers.org/hco/1/GRCh38#101021803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115686314-C-A

101021803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686314-C-G

101021803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686314-C-T

101021805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686312-G-A

101021805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686312-G-C

101021805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686312-G-T

http://identifiers.org/hco/1/GRCh38#101021841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115686277-C-A

101021841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686277-C-G

101021841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686277-C-T

101021845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686273-C-T

101021902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686201-G-T

101021999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686103-G-A

101021999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115686103-G-T

101022173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115685961-G-A

101022207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115685919-A-G

101022285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115685846-C-T

101022504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115685694-T-C

101022628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115685629-T-C

101023489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115683881-T-G

101024449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115683113-T-C

101024538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115682979-A-T

101024657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115682832-T-C

101024668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115682805-C-G

101024842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115682703-T-C

101024868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115682682-G-T

http://identifiers.org/hco/1/GRCh38#101024963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115682581-C-A

http://identifiers.org/hco/1/GRCh38#101025004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#115682540-C-A

101025152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115682393-A-G

101025535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115682020-G-A

101025535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115682020-G-T

101025625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115681946-T-G

101025724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115681883-T-C

101025739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115681868-T-C

101025739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115681868-T-G

101025740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115681867-T-A

101025740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115681867-T-C

101025776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115681833-A-G

101025776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115681833-A-T

101025777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115681832-G-A

101025777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115681832-G-C

101025777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115681832-G-T

101025836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115681777-T-C

101025836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115681777-T-G

101025872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115681728-G-A

101025872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115681728-G-T

101025873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115681727-G-C

101025873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115681727-G-T

101025928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115681675-C-T

101025935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115681668-A-G

101026033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24270
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115681593-T-C