http://identifiers.org/hco/10/GRCh38#97356392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41851005-C-A

http://identifiers.org/hco/10/GRCh38#97356496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41851154-C-A

97356496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851154-C-T

97356506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851164-T-C

97356597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851247-T-C

97356597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851247-T-G

http://identifiers.org/hco/10/GRCh38#97356622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41851272-C-A

97356758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851354-A-G

97356758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851354-A-T

97356878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851429-G-T

97356903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851454-G-C

97356903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851454-G-T

97356913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851464-T-C

97356921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851472-G-T

http://identifiers.org/hco/10/GRCh38#97356997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41851550-C-A

97357006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851559-T-A

97357045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851593-C-T

97357076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851626-G-A

97357076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851626-G-T

97357081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851641-G-T

97357082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851642-G-A

97357082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41851642-G-T

97357420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41852022-C-T

97357483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41852080-T-C

97357680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41852294-T-C

97358784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41853854-T-C

97358871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41853914-A-T

97359033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854050-T-C

97359112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854125-A-G

97359112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854125-A-T

97359119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854133-G-T

97359992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854746-G-C

97360318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854934-T-A

http://identifiers.org/hco/10/GRCh38#97360363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41854981-C-A

97360406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855029-T-A

97360406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855029-T-C

97360515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855117-G-T

97360528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855127-G-A

97360528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855127-G-C

97360528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855127-G-T

http://identifiers.org/hco/10/GRCh38#97360574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41855173-C-A

97360574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41855173-C-T

97360637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855232-T-C

97360638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855233-G-T

97362236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41856195-G-A

97362361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41856309-G-A

97362432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41856384-G-A

97362432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41856384-G-C

97362455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41856423-T-C

97363860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41857215-G-T

http://identifiers.org/hco/10/GRCh38#97363999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41857347-C-A

97363999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41857347-C-T

97364325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41857732-G-C

97364923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41858093-G-A

97364977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41858130-A-G

97366067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 41859177-A-G

97366318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41859445-G-A

97366318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41859445-G-T

97366390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41859518-A-T

http://identifiers.org/hco/10/GRCh38#97366405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41859533-C-A

97366495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41859623-C-T

97366588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41859710-C-G

97366704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41859822-G-A

97366704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41859822-G-C

97366704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41859822-G-T

97366723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41859841-G-A

97366768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41859887-C-T

97366803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41859922-C-T

97366882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41860001-G-A

97366882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41860001-G-T

97366928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860047-G-A

97366928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860047-G-C

97366983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860098-G-T

97367009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860135-G-A

97367009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860135-G-T

97367191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41860326-A-G

97367197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41860332-G-C

97367197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41860332-G-T

97367233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41860367-G-A

97367233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41860367-G-T

http://identifiers.org/hco/10/GRCh38#97367276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41860413-C-A

97367276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41860413-C-T

97367284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41860421-T-C

http://identifiers.org/hco/10/GRCh38#97367325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41860459-C-A

97367325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41860459-C-T

97367472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860559-A-G

97367493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860581-T-C

97367510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860598-T-C

97367510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860598-T-G

http://identifiers.org/hco/10/GRCh38#97367541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41860622-A-C

97367541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860622-A-G

97369051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861057-G-T

97369157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861145-A-T

97369306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861238-T-A

97369306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861238-T-C

97369329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861261-A-G

http://identifiers.org/hco/10/GRCh38#97369357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41861286-C-A

97369357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861286-C-T

http://identifiers.org/hco/10/GRCh38#97369391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41861315-C-A

97369391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861315-C-T

97369409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861331-G-T

97369434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41861357-C-T

97369437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41861360-A-G

97369449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41861372-G-A

97369449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41861372-G-C

97369473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41861396-T-A

97369473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41861396-T-C

97369476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41861399-C-T

97369494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41861417-T-A

97369494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41861417-T-G

97369497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41861420-A-G

http://identifiers.org/hco/10/GRCh38#97369621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41861552-A-C

http://identifiers.org/hco/10/GRCh38#97369629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41861560-C-A

97369629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861560-C-G

97369630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861561-A-G

http://identifiers.org/hco/10/GRCh38#97369722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41861713-C-A

97369722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861713-C-G

97369722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861713-C-T

97369868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861927-G-A

97369983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862014-T-C

97370011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862041-G-A

97370011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862041-G-T

97370025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862053-A-G

97370088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862114-A-G

http://identifiers.org/hco/10/GRCh38#97370128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41862155-C-A

97370213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41862228-G-A

97370213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41862228-G-C

97370213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41862228-G-T

97370327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862342-G-C

97370327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862342-G-T

97370333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862348-G-A

97370333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862348-G-T

97370334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862349-G-A

97370334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862349-G-T

97370389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862413-T-C

97370391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862501-G-T

97370396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862506-G-A

97370396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862506-G-T

97370397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862507-T-G

97370440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862655-C-G

97370440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862655-C-T

97370447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41862662-G-A

97370447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41862662-G-T

http://identifiers.org/hco/10/GRCh38#97370672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41862924-C-A

97370672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862924-C-T

97370837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863088-C-T

97370899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863133-A-G

97370911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863144-T-C

97370920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863153-C-G

97370920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863153-C-T

97370945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41863178-C-T

97371010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41863243-G-A

97371073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41863306-G-A

97371144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41863389-A-G

97371712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864706-G-A

97371712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864706-G-C

97371712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864706-G-T

97371732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864728-A-G

97371826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864818-G-A

97371826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864818-G-T

http://identifiers.org/hco/10/GRCh38#97371828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41864820-C-A

97371828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864820-C-T

http://identifiers.org/hco/10/GRCh38#97371914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41864887-C-A

97371914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864887-C-T

97371918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864891-A-G

http://identifiers.org/hco/10/GRCh38#97371970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41864938-C-A

97371970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41864938-C-T

97372195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865093-G-C

97372195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865093-G-T

97372269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865131-G-C

97372269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865131-G-T

97372300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865174-G-C

97372317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865191-A-G

97372485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865349-G-A

http://identifiers.org/hco/10/GRCh38#97372584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41865420-C-A

97372584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865420-C-T

http://identifiers.org/hco/10/GRCh38#97372622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41865452-A-C

97372623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865453-T-C

97372651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865469-G-C

97372651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865469-G-T

http://identifiers.org/hco/10/GRCh38#97372670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41865486-C-A

http://identifiers.org/hco/10/GRCh38#97372684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41865498-C-A

97372684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865498-C-T

97372687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865501-C-G

97372687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865501-C-T

97372724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865529-T-A

97372724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865529-T-C

97372794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41865598-T-C

97372794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41865598-T-G

97372942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865712-A-G

97373052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41865781-G-A

97373052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41865781-G-C

97373052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41865781-G-T

97373079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41865808-G-A

97373079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41865808-G-T

http://identifiers.org/hco/10/GRCh38#97373190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41865919-A-C

97373229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865958-A-T

http://identifiers.org/hco/10/GRCh38#97373545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41866206-C-A

97373545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866206-C-T

97373603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41866251-G-A

97373753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866396-A-T

97373766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866415-G-A

http://identifiers.org/hco/10/GRCh38#97373822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41866460-A-C

97373822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41866460-A-G

http://identifiers.org/hco/10/GRCh38#97373828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41866466-A-C

97373842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41866480-T-C

97373997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866634-G-T

97374083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866810-C-T

97374169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866877-T-C

97374199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866923-T-C

97374210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866934-C-T

97374231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866952-G-A

97374271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866984-G-A

97374388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41867153-C-G

http://identifiers.org/hco/10/GRCh38#97379227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41868472-C-A

97379240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41868485-G-T

http://identifiers.org/hco/10/GRCh38#97379268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41868518-A-C

97379268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41868518-A-G

97379269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41868519-C-T

97379275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41868525-G-A

97379552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41868725-C-T

97379589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41868759-C-G

97379699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 41868869-C-G

http://identifiers.org/hco/10/GRCh38#97379843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41869176-C-A

97379843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869176-C-G

97379843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869176-C-T

97379863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869195-G-A

97379863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869195-G-T

97379892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869217-C-T

97379915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869241-C-T

97379918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869244-G-A

97379918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869244-G-C

97379919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869245-T-C

97379958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869287-T-C

http://identifiers.org/hco/10/GRCh38#97379964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41869293-A-C

97379964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869293-A-G

97380101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869425-C-T

97380696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870498-G-A

97380696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870498-G-T

97380698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870500-G-A

97380698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870500-G-T

97380711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870509-G-T

http://identifiers.org/hco/10/GRCh38#97380724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41870518-C-A

97380724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870518-C-T

97380777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870576-G-A

97380777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870576-G-T

97380787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870586-C-T

97380817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41870616-G-C

97380817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41870616-G-T

97380847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: 41870646-A-G

http://identifiers.org/hco/10/GRCh38#97380975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41870761-A-C

http://identifiers.org/hco/10/GRCh38#97381060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41870843-A-C

97381060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41870843-A-G

http://identifiers.org/hco/10/GRCh38#97381514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41871987-C-A

97381599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872058-A-T

http://identifiers.org/hco/10/GRCh38#97381613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41872071-C-A

97381613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872071-C-T

97381754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: 41872191-T-C

97381757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: 41872194-G-A

97381757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: 41872194-G-C

97381784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: 41872221-A-G

http://identifiers.org/hco/10/GRCh38#97381808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41872245-C-A

97381808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: 41872245-C-T

97381823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: 41872260-C-T

97381833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41872270-A-G

http://identifiers.org/hco/10/GRCh38#97381838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41872275-A-C

97381842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872279-G-A

97381842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872279-G-T

97381851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872288-G-C

97381851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872288-G-T

97381866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872381-C-T

97381871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872386-G-A

97381890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872405-T-A

97381890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872405-T-C

http://identifiers.org/hco/10/GRCh38#97381931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41872420-C-A

97381931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872420-C-G

97381931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872420-C-T

97381933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872422-G-A

97381933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872422-G-C

97381933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41872422-G-T

97383976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41873943-C-T

97385159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41874079-T-A

97385775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41874432-G-T

http://identifiers.org/hco/10/GRCh38#97385786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41874443-C-A

97385786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41874443-C-G

97385786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41874443-C-T

http://identifiers.org/hco/10/GRCh38#97385791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41874448-C-A

97385791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41874448-C-T

97385797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41874454-T-C

97385805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41874463-T-C

97385815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41874472-G-A

97385815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41874472-G-T

http://identifiers.org/hco/10/GRCh38#97386065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41874694-C-A

97386065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41874694-C-T

97388312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41875299-C-T

97388330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41875317-G-A

97388535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: 41875496-G-A

http://identifiers.org/hco/10/GRCh38#97388649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41875611-C-A

97388649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41875611-C-T

97388657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41875619-G-A

97388784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41875707-C-G

97388934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41875815-C-T

97390426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 41878208-G-C

97390613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41878391-T-C

97390671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41878459-T-C

97390732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41878501-C-T

97390748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 41878517-G-T

97390808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, missense_variant
orthologous variants: 41878577-A-T

97390852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41878621-A-G

97390933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41878687-G-A

http://identifiers.org/hco/10/GRCh38#97390937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41878691-C-A

97390937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41878691-C-G

97390937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41878691-C-T

97391022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41878773-C-T

http://identifiers.org/hco/10/GRCh38#97391062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41878823-A-C

97391062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41878823-A-G

97391169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41879026-A-G

97393716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 41879555-G-A

97393716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 41879555-G-C

97393814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41879651-A-G

97393838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41879687-G-T

97393867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41879716-A-G

97393896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41879745-G-T

http://identifiers.org/hco/10/GRCh38#97395572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41880132-C-A

97395625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41880184-C-T

97395707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41880320-C-T

97395912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41880534-A-G

http://identifiers.org/hco/10/GRCh38#97396193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41880953-C-A

97396193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41880953-C-T

http://identifiers.org/hco/10/GRCh38#97396194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41880954-C-A

97396220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 41880979-G-A

97396220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 41880979-G-T

97396242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 41881001-C-T

97396355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881122-G-A

97396370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881130-T-C

97396540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881296-T-C

http://identifiers.org/hco/10/GRCh38#97396576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41881311-C-A

97396655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881361-C-T

97396890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881606-A-G

97396909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881624-T-A

97396932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881646-T-C

97397009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881712-C-T

97397017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881720-A-G

97397055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881760-A-T

97398694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881785-G-C

97398694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881785-G-T

97398705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881796-T-C

97398856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881899-G-T

97398871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41881913-T-A

http://identifiers.org/hco/10/GRCh38#97399053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41882149-C-A

97399053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41882149-C-T

97399418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41882645-T-C

97399430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41882657-T-C

97400443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: synonymous variant
orthologous variants: 41883725-C-T

http://identifiers.org/hco/10/GRCh38#97400579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41883873-C-A

97400579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41883873-C-G

97400579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41883873-C-T

97400656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41883947-A-G

97400703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41883992-G-A

97400893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron variant
orthologous variants: 41884240-C-T

http://identifiers.org/hco/10/GRCh38#97400941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41884285-A-C

97401036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, undefined
orthologous variants: 41884350-G-C

97401036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, undefined
orthologous variants: 41884350-G-T

97401152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41884437-T-C

http://identifiers.org/hco/10/GRCh38#97401285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41884569-A-C

97401285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41884569-A-G

97401285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41884569-A-T

http://identifiers.org/hco/10/GRCh38#97401294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41884590-C-A

97401294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41884590-C-G

97401294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41884590-C-T

http://identifiers.org/hco/10/GRCh38#97401470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41884750-A-C

97401500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41884777-G-A

97401500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41884777-G-T

http://identifiers.org/hco/10/GRCh38#97401510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41884787-C-A

97401510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41884787-C-T

97401551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884878-G-A

97401551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884878-G-T

97401567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884894-G-A

http://identifiers.org/hco/10/GRCh38#97401631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41884966-C-A

97401701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885055-G-A

97402180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885223-C-T

97402181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885224-G-A

97402181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885224-G-T

97408633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41889054-G-C

97408674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41889096-T-C

97418656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41895021-G-T

http://identifiers.org/hco/10/GRCh38#97418779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41895104-A-C

97418982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41895223-T-C

97418990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41895230-T-C

97418990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41895230-T-G

97419034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41895273-G-A

97419034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41895273-G-T

97419061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41895300-A-T

97419138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41895367-T-A

97419138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41895367-T-C

97419147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41895376-C-T

97419208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41895434-G-T

http://identifiers.org/hco/10/GRCh38#97419212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41895438-C-A

97419222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41895456-G-A

97419222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41895456-G-C

97419222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41895456-G-T

97419272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41895511-T-C

97419272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41895511-T-G

http://identifiers.org/hco/10/GRCh38#97419275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41895514-C-A

http://identifiers.org/hco/10/GRCh38#97419279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41895518-A-C

97419283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41895522-T-C

97419283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41895522-T-G

97419313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41895552-G-A

97419313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41895552-G-T

97419334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41895564-G-C

97419334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41895564-G-T

97419351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41895581-T-C

97419376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41895606-T-C

http://identifiers.org/hco/10/GRCh38#97419448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41895677-C-A

97419448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41895677-C-T

97420074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41895936-T-C

97422933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41896524-C-T

97423094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41896667-T-C

97423133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41896694-A-T

97424749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41899050-A-G

97424753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41899054-T-C

97424753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41899054-T-G

http://identifiers.org/hco/10/GRCh38#97425735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41900006-C-A

97425735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41900006-C-G

97425735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41900006-C-T

97425968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900145-T-A

97425968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900145-T-C

97425968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900145-T-G

97425970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900147-C-T