http://identifiers.org/hco/11/GRCh38#133896706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27268575-C-A

133896725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27268556-G-A

133896972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27268329-T-C

133897007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27268296-A-G

133897090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27268213-T-C

133897157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27268143-G-T

133897215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27268088-C-T

http://identifiers.org/hco/11/GRCh38#133897287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27268018-C-A

133897364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27267960-G-A

133897451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27267884-G-T

http://identifiers.org/hco/11/GRCh38#133897504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27267830-C-A

133897504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27267830-C-G

133897541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27267793-G-C

133897541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27267793-G-T

133897586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27267751-C-T

http://identifiers.org/hco/11/GRCh38#133897889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27267472-C-A

133897889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27267472-C-T

http://identifiers.org/hco/11/GRCh38#133897966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27267355-A-C

133897966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27267355-A-G

http://identifiers.org/hco/11/GRCh38#133898257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27267061-C-A

133898257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27267061-C-T

133898393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266935-A-G

133898466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266860-A-G

133898472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266854-A-G

133898491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266835-A-G

133898493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266833-A-G

http://identifiers.org/hco/11/GRCh38#133898500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27266826-C-A

133898500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266826-C-T

133898509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27266817-A-G

133898777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266551-T-C

http://identifiers.org/hco/11/GRCh38#133898858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27266486-C-A

133898858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266486-C-T

http://identifiers.org/hco/11/GRCh38#133898939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27266417-C-A

133898939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266417-C-T

http://identifiers.org/hco/11/GRCh38#133899009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27266347-C-A

133899027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266329-G-T

133899164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266198-G-A

133899164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266198-G-T

http://identifiers.org/hco/11/GRCh38#133899172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27266190-C-A

133899172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266190-C-T

133899285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266090-G-T

133899299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266076-T-A

133899299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266076-T-C

133899315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266063-T-G

http://identifiers.org/hco/11/GRCh38#133899327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27266050-C-A

133899358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27266015-T-C

133899372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265998-A-G

133899372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265998-A-T

http://identifiers.org/hco/11/GRCh38#133899435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27265931-C-A

http://identifiers.org/hco/11/GRCh38#133899578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27265809-C-A

http://identifiers.org/hco/11/GRCh38#133899688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27265663-C-A

133899688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265663-C-T

133899707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265644-A-G

http://identifiers.org/hco/11/GRCh38#133899814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27265559-C-A

http://identifiers.org/hco/11/GRCh38#133899933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27265472-C-A

133899933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265472-C-T

133899970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265426-A-G

133900071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265355-G-A

133900071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265355-G-T

133900099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265327-T-C

http://identifiers.org/hco/11/GRCh38#133900125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27265301-C-A

http://identifiers.org/hco/11/GRCh38#133900126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27265300-C-A

133900144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265254-G-T

133900167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265231-T-C

133900215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265208-G-A

133900394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265036-G-T

133900419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27265009-A-G

133900428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264999-A-G

133900429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264998-T-C

133900514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264922-C-T

133900557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264881-A-G

http://identifiers.org/hco/11/GRCh38#133900571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27264868-C-A

133900577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264861-G-A

133900586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264852-A-G

133900620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264829-C-T

http://identifiers.org/hco/11/GRCh38#133900624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27264825-C-A

133900633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264816-A-G

133900666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264783-A-G

133900820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264629-C-T

133900823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264626-A-G

133900823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264626-A-T

http://identifiers.org/hco/11/GRCh38#133900826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27264623-C-A

133900826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264623-C-T

133900855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264594-A-G

133900920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264541-T-C

133901002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264462-G-A

133901002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264462-G-T

http://identifiers.org/hco/11/GRCh38#133901086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27264378-C-A

133901096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264371-G-A

http://identifiers.org/hco/11/GRCh38#133901147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27264344-C-A

133901147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264344-C-T

133901413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27264048-T-C

133901785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27263673-C-T

133902927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27263237-C-T

http://identifiers.org/hco/11/GRCh38#133903012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27263142-A-C

133903412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27262758-C-T

133903467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27262707-T-A

133903482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27262693-T-C

133903778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27262391-C-T

http://identifiers.org/hco/11/GRCh38#133904146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27262038-C-A

133904146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27262038-C-T

133904973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27261697-G-A

133905115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27261578-C-G

133905133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27261559-G-T

133905137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27261555-C-G

133905818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27260527-C-T

133906248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27260064-C-T

http://identifiers.org/hco/11/GRCh38#133906263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27260049-A-C

133906288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27260024-T-C

133906318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27259994-G-A

http://identifiers.org/hco/11/GRCh38#133906461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27259827-A-C

133906778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27259496-T-C

133906778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27259496-T-G

133906790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27259484-C-T

133906906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27259392-G-A

133906948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27259355-C-T

133907149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27259163-A-T

http://identifiers.org/hco/11/GRCh38#133907372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27258938-C-A

133907584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258772-C-T

http://identifiers.org/hco/11/GRCh38#133907607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27258744-C-A

133907607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258744-C-T

133907608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258743-G-A

http://identifiers.org/hco/11/GRCh38#133907650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27258700-C-A

133907944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258409-T-C

133908004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258349-G-A

133908034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258329-G-T

133908086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258273-C-T

133908166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258184-C-G

133908186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258162-G-C

http://identifiers.org/hco/11/GRCh38#133908187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27258161-C-A

133908187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258161-C-T

133908239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258108-G-A

133908241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258106-T-C

133908331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3 prime UTR variant
orthologous variants: 27258011-C-G

http://identifiers.org/hco/11/GRCh38#133908740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27257621-C-A

133908740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27257621-C-G

133908899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27257451-G-A

133908899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27257451-G-T

http://identifiers.org/hco/11/GRCh38#133909018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27257325-C-A

133909040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27257301-G-A

133909040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27257301-G-T

133909402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27256941-A-G

133909679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27256678-T-C

133909725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27256632-G-C

133910966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27254749-A-G

133911500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27254272-A-T

http://identifiers.org/hco/11/GRCh38#133911550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27254224-A-C

http://identifiers.org/hco/11/GRCh38#133911793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27253987-C-A

133912111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27253706-T-A

133912111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27253706-T-C

133912334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27253491-A-T

133912455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27253387-T-C

133912695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27253150-C-T

133912817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27253019-T-C

133913269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27252563-C-T

133913354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27252476-A-T

133913500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27252341-G-A

http://identifiers.org/hco/11/GRCh38#133913587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27252253-C-A

133913628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27252211-G-A

133913628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27252211-G-C

133913910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27251946-C-T

http://identifiers.org/hco/11/GRCh38#133914276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27251391-C-A

133914594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27251150-C-T

133915292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27250458-A-G

133915292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27250458-A-T

133915656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27250151-A-G

133916223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27249530-G-A

133916343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27249409-G-A

133916343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27249409-G-C

133916503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27249244-G-C

http://identifiers.org/hco/11/GRCh38#133917068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27248630-C-A

133917068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27248630-C-G

133917112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27248585-A-G

133917293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27248406-G-A

http://identifiers.org/hco/11/GRCh38#133917732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27248015-C-A

133917732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27248015-C-G

133917732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27248015-C-T

133917908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27247819-G-A

http://identifiers.org/hco/11/GRCh38#133918214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27247499-C-A

133918214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27247499-C-G

133918214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27247499-C-T

133918384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27247333-G-C

133918497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27247217-G-A

133918845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246878-G-A

133918849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246874-G-A

133918905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246806-G-T

133918916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246798-G-A

133918916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246798-G-T

133918953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246760-G-A

133918953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246760-G-C

133918953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246760-G-T

http://identifiers.org/hco/11/GRCh38#133919088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27246644-C-A

133919088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, missense_variant
orthologous variants: 27246644-C-G

133919088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, missense_variant
orthologous variants: 27246644-C-T

133919143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246583-T-A

133919143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246583-T-C

133919143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246583-T-G

133919516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246236-A-G

133919574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246181-G-C

133919612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246147-G-A

133919612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246147-G-T

http://identifiers.org/hco/11/GRCh38#133919613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27246146-A-C

http://identifiers.org/hco/11/GRCh38#133919620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27246139-C-A

133919620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246139-C-T

133919632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246130-G-A

133919632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246130-G-C

133919632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246130-G-T

http://identifiers.org/hco/11/GRCh38#133919645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27246116-C-A

133919645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27246116-C-T

133919805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense variant
orthologous variants: 27245967-G-A

133919805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense variant
orthologous variants: 27245967-G-T

133919812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense variant
orthologous variants: 27245960-G-A

133919812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense variant
orthologous variants: 27245960-G-C

133919812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense variant
orthologous variants: 27245960-G-T

133920378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense variant
orthologous variants: 27245391-G-A

133920378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense variant
orthologous variants: 27245391-G-T

133921194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense variant
orthologous variants: 27244575-G-A

133921476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27244299-A-G

133921712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27244213-A-T

http://identifiers.org/hco/11/GRCh38#133921950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27243999-C-A

133922096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243923-T-A

133922134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243882-C-T

133922146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243872-G-A

133922285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243708-T-A

133922285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243708-T-C

133922321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243666-A-G

133922321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243666-A-T

133922422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243537-T-G

http://identifiers.org/hco/11/GRCh38#133922433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27243526-C-A

133922434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243525-T-C

133922489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243182-G-A

133922489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243182-G-T

133922521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243144-C-T

http://identifiers.org/hco/11/GRCh38#133922558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27243117-C-A

133922558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243117-C-G

133922558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27243117-C-T

http://identifiers.org/hco/11/GRCh38#133922678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27242997-C-A

133922678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27242997-C-T

133922703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27242972-T-C

133922718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27242957-T-C

http://identifiers.org/hco/11/GRCh38#133922755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27242920-A-C

133922755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27242920-A-G

133922755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27242920-A-T

http://identifiers.org/hco/11/GRCh38#133922792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27242879-C-A

133922792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27242879-C-T

133922842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27242837-A-G

http://identifiers.org/hco/11/GRCh38#133922863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27242816-C-A

133922863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27242816-C-T

133923103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27242596-T-C

133923262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27242489-G-A

133923908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27241849-T-C

133924649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27241096-T-C

http://identifiers.org/hco/11/GRCh38#133924687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27241052-C-A

133924687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27241052-C-T

133924799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240939-A-G

133924800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240938-G-A

133924800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240938-G-T

133924961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240777-C-T

http://identifiers.org/hco/11/GRCh38#133924964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27240774-C-A

http://identifiers.org/hco/11/GRCh38#133924998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27240761-C-A

133924998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240761-C-T

http://identifiers.org/hco/11/GRCh38#133925006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27240753-C-A

133925006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240753-C-T

133925008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240751-A-G

133925010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240749-A-G

133925164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240591-C-T

133925524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240225-G-A

133925652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240097-G-T

133925661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240088-T-C

133925724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27240023-G-T

133926331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238754-C-T

133926702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238540-A-G

http://identifiers.org/hco/11/GRCh38#133926785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27238456-C-A

133926785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238456-C-G

http://identifiers.org/hco/11/GRCh38#133926816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27238426-A-C

133926816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238426-A-G

133926816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238426-A-T

133926819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238423-T-C

133926831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238411-G-A

133926831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238411-G-T

133926855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238392-G-A

133926855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238392-G-T

133926863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238384-G-A

133926863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238384-G-T

http://identifiers.org/hco/11/GRCh38#133926867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27238380-C-A

133926867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238380-C-G

133926867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238380-C-T

133926906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238325-G-A

133926906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238325-G-C

133926906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238325-G-T

133927200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238027-G-A

133927200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27238027-G-T

133927240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27237988-T-C

133927321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27237908-G-A

http://identifiers.org/hco/11/GRCh38#133927648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27237581-A-C

133927888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27237317-G-A

133927954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27236751-C-T

133928103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27236619-G-A

133928410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27236416-C-G

133928410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27236416-C-T

133928835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27236085-G-C

133928862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27236065-A-G

133929829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27235425-G-A

133929829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27235425-G-T

http://identifiers.org/hco/11/GRCh38#133929841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27235413-C-A

133929841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27235413-C-G

133929841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27235413-C-T

133930025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27235247-T-C

133930058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27235220-C-T

133930178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27235153-T-C

133930484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234966-C-T

http://identifiers.org/hco/11/GRCh38#133930711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27234812-C-A

133930711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234812-C-T

133930849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234729-T-G

http://identifiers.org/hco/11/GRCh38#133930859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27234719-A-C

133930859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234719-A-T

133930874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234704-G-A

133930874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234704-G-C

133930874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234704-G-T

133930901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27234690-G-A

133930901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27234690-G-T

http://identifiers.org/hco/11/GRCh38#133930939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27234670-C-A

133930939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234670-C-G

133930939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234670-C-T

133930944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234665-T-A

133930944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234665-T-C

133930975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234662-G-A

133931012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27234625-G-A

133931012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27234625-G-C

133931166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234470-G-C

133931205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234409-G-A

133931239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234375-G-A

133931239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27234375-G-T

http://identifiers.org/hco/11/GRCh38#133931425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27234282-C-A

http://identifiers.org/hco/11/GRCh38#133931818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27233888-C-A

133931831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27233875-T-G

133931877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27233819-G-T

133931970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27233709-G-A

133931970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27233709-G-T

133932052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27233628-A-G

http://identifiers.org/hco/11/GRCh38#133933780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27232873-C-A

133933913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27232738-G-A

133933970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27232681-T-C

133933984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27232634-T-G

133933988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27232630-T-C

133934379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27232211-T-C

133934595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27231998-G-T

133934625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27231972-C-T

http://identifiers.org/hco/11/GRCh38#133935002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#27231578-C-A

133935139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27231446-C-T

133935196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27231369-G-A

133935470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27231092-G-A

133935470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27231092-G-T

133935875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27230715-T-C

133935875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27230715-T-G

133936567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27230155-G-C

133936770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27229996-G-A

http://identifiers.org/hco/11/GRCh38#133937231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27229363-C-A

133937231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27229363-C-T

133937248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27229341-G-A

133937248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27229341-G-T

133937566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27229034-G-A

133937566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27229034-G-T

http://identifiers.org/hco/11/GRCh38#133937597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27229008-C-A

133937605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27229000-G-T

133937667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27228952-G-A

133937667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27228952-G-C

http://identifiers.org/hco/11/GRCh38#133937672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27228947-C-A

133937672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27228947-C-T

133937701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27228917-G-T

133937707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27228911-T-C

133937711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27228907-T-C

http://identifiers.org/hco/11/GRCh38#133937752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27228859-C-A

133937752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27228859-C-T

http://identifiers.org/hco/11/GRCh38#133937781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27228832-C-A

http://identifiers.org/hco/11/GRCh38#133937819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27228791-C-A

133937819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27228791-C-T

133938030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27228545-T-C

133938137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27228386-T-A

133938137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27228386-T-C

http://identifiers.org/hco/11/GRCh38#133938194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27228316-C-A

133938194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27228316-C-T

http://identifiers.org/hco/11/GRCh38#133938211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27228295-C-A

133938211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27228295-C-T

133938553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27227960-T-C

133938597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27227916-G-C

133938964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: -G-A

133939233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: -T-C

133940866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27226321-G-A

133941640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27225569-G-A

133942103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27225112-C-T

133942235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27224983-T-G

133942697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27224517-T-A

133942837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27224372-A-G

http://identifiers.org/hco/11/GRCh38#133943090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27223848-A-C

133943116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27223822-C-T

133943152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27223786-C-T

133944052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27223139-G-A

133944144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27223059-G-A

133944144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27223059-G-T

133944376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27222851-T-C

133944390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27222838-G-A

133944390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27222838-G-C

133944390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27222838-G-T

133944461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27222755-T-A

133944461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27222755-T-C

http://identifiers.org/hco/11/GRCh38#133944479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27222737-C-A

http://identifiers.org/hco/11/GRCh38#133944481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27222735-A-C

133944579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27222613-A-T

133944877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27222347-A-T

133944953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27222278-C-T

133945311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27221728-T-C

http://identifiers.org/hco/11/GRCh38#133945750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27221270-C-A

133945772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27221252-C-G

133945963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27221019-A-G

133945963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27221019-A-T

133945983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220999-G-T

133946027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220943-G-A

133946027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220943-G-T

133946033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220937-T-C

133946033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220937-T-G

133946046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220910-G-A

http://identifiers.org/hco/11/GRCh38#133946049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27220907-C-A

133946049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220907-C-T

133946265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 27220691-G-A

133946291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, missense_variant
orthologous variants: 27220666-G-T

http://identifiers.org/hco/11/GRCh38#133946349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27220616-C-A

133946349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220616-C-T

http://identifiers.org/hco/11/GRCh38#133946355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27220610-A-C

133946402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220569-G-A

133946402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220569-G-T

http://identifiers.org/hco/11/GRCh38#133946438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27220538-C-A

133946438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220538-C-G

133946438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220538-C-T

133946604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27220377-C-T

133947199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27219788-C-T

133947288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, undefined
orthologous variants: 27219697-G-A

133947677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, undefined
orthologous variants: 27219377-C-T

133947840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27219225-G-A

133947850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27219221-C-G

133947850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27219221-C-T

133948666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27218403-T-C

http://identifiers.org/hco/11/GRCh38#133948993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27218096-C-A

133949050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27218021-G-C

133949144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27217919-G-C

133949269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27217798-G-C

133949460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27217592-A-G

133949893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27217183-T-C

133949893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27217183-T-G

133950207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27216904-C-T

133950653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27216577-G-A

133951390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27215860-G-A

133951443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27215813-G-C

133951505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27215756-C-T

133951597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27215672-C-T

133951638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27215631-G-A

http://identifiers.org/hco/11/GRCh38#133951813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27215481-C-A

133951831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27215469-G-C

133951831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27215469-G-T

133951955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 27215359-G-A

133951955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, stop_gained
orthologous variants: 27215359-G-T

133952012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 27215302-G-A

133952012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 27215302-G-C

133952012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 27215302-G-T

133952035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron_variant, missense_variant
orthologous variants: 27215276-G-T

133952570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27214640-G-T

133952793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27214494-A-G

133952797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27214490-A-G

133953052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27214173-G-A

133953073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27214152-G-A

133953138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27214093-C-T

133953152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27214079-G-A

133953210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27214017-C-T

133953596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27213665-A-G

133953604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27213657-G-T

http://identifiers.org/hco/11/GRCh38#133953627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27213634-C-A

133953771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27213504-C-G

133954197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27213012-C-T

133954326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27212936-C-T

133954384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27212880-G-C

133954384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27212880-G-T

133954548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27212736-A-G

133954617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27212667-A-G

133955054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27212254-C-T

http://identifiers.org/hco/11/GRCh38#133955568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27211783-C-A

133955568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27211783-C-G

133955784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27211585-C-T

http://identifiers.org/hco/11/GRCh38#133955789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27211580-C-A

133955872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27211501-G-T

http://identifiers.org/hco/11/GRCh38#133955921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27211467-C-A

133955943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27211445-T-G

133955997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27211410-G-C

133956059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27211347-G-C

133956103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27211312-G-A

133956103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27211312-G-C

133956160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27211256-G-A

133956590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27210886-T-C

http://identifiers.org/hco/11/GRCh38#133956643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#27210859-C-A

133956643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27210859-C-G

133956643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: intron variant
orthologous variants: 27210859-C-T

133956868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27210642-G-A

133956868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32326
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27210642-G-T