http://identifiers.org/hco/8/GRCh38#141207274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73449369-C-A

141207274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73449369-C-T

141207673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73449728-C-T

141207708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73449738-A-G

141207842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73449870-G-A

141207842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73449870-G-T

141208001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73449981-T-A

141208001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73449981-T-C

141208045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450014-A-T

141208163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450128-G-A

141208235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450192-T-C

141208440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450323-G-C

141208479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450341-T-C

141208540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450382-G-T

http://identifiers.org/hco/8/GRCh38#141208661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73450480-C-A

141208661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450480-C-G

141208661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450480-C-T

141208668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450487-C-G

http://identifiers.org/hco/8/GRCh38#141208723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73450536-C-A

http://identifiers.org/hco/8/GRCh38#141208724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73450537-C-A

141208724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450537-C-G

141208943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450659-A-G

141208952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450668-A-G

http://identifiers.org/hco/8/GRCh38#141209017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73450712-C-A

141209017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450712-C-T

141209056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450753-G-A

141209056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450753-G-T

141209097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450780-C-T

141209128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450811-G-T

141209135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450814-A-G

141209160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450850-T-C

141209297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73450985-T-C

http://identifiers.org/hco/8/GRCh38#141209326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73451014-C-A

141209449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451115-G-A

http://identifiers.org/hco/8/GRCh38#141209701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73451341-C-A

http://identifiers.org/hco/8/GRCh38#141209715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73451355-A-C

141209716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451356-T-C

141209716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451356-T-G

http://identifiers.org/hco/8/GRCh38#141209823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73451455-C-A

141209823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451455-C-T

141209829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451461-G-T

http://identifiers.org/hco/8/GRCh38#141209868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73451496-C-A

141209868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451496-C-T

141210107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451696-A-G

141210178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451739-A-G

http://identifiers.org/hco/8/GRCh38#141210289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73451835-C-A

141210289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451835-C-T

http://identifiers.org/hco/8/GRCh38#141210374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73451913-C-A

141210374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73451913-C-T

141210518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452057-A-G

141210729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452260-A-G

141210929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452454-T-A

141210929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452454-T-C

141210929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452454-T-G

141210932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452457-T-A

141210932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452457-T-C

141210932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452457-T-G

141210943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452468-A-G

141210952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452475-G-A

141210952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452475-G-T

http://identifiers.org/hco/8/GRCh38#141210955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73452478-C-A

141210955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452478-C-T

141210956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452479-G-A

141210956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452479-G-T

141210963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452499-T-C

141211019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452568-G-A

141211019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452568-G-T

http://identifiers.org/hco/8/GRCh38#141211088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73452670-C-A

141211088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452670-C-T

141211201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452784-G-C

141211201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452784-G-T

http://identifiers.org/hco/8/GRCh38#141211249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73452810-C-A

141211249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452810-C-G

141211249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452810-C-T

141211280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452834-T-C

141211280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452834-T-G

http://identifiers.org/hco/8/GRCh38#141211386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73452927-C-A

141211386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452927-C-G

141211386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3 prime UTR variant
orthologous variants: 73452927-C-T

141211532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 73453052-T-A

141211556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 73453066-A-G

141211654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 73453160-A-G

141212091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 73453558-G-A

141212091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 73453558-G-T

http://identifiers.org/hco/8/GRCh38#141212152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73453580-C-A

141212152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 73453580-C-G

141212152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 73453580-C-T

http://identifiers.org/hco/8/GRCh38#141212179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73453607-C-A

141212179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 73453607-C-T

141212287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: missense variant
orthologous variants: 73453710-T-A

141212287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 73453710-T-C

141212376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 73453799-G-A

141212376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: missense variant
orthologous variants: 73453799-G-T

141212401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 73453824-G-A

141212583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73454004-G-A

141212583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73454004-G-T

141212632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73454053-T-G

141212652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73454070-A-G

141212662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73454080-T-C

141215963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: synonymous variant
orthologous variants: 73456391-T-C

141215980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73456408-G-T

141216025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73456430-G-T

http://identifiers.org/hco/8/GRCh38#141216034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73456439-C-A

141216034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73456439-C-T

141216045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73456450-C-T

http://identifiers.org/hco/8/GRCh38#141216058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73456463-C-A

141216058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73456463-C-T

http://identifiers.org/hco/8/GRCh38#141216078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73456472-C-A

141216078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73456472-C-T

141216503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73456748-A-T

141216547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73456780-C-G

141216851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457038-G-T

141216952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457090-G-A

141216952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457090-G-T

141217044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457109-G-T

141217209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457253-G-A

141217234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457273-C-T

141217238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457277-C-T

http://identifiers.org/hco/8/GRCh38#141217250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73457291-C-A

141217250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457291-C-T

http://identifiers.org/hco/8/GRCh38#141217257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73457298-C-A

141217335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457320-A-G

141217513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457461-C-T

141217576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457498-A-G

http://identifiers.org/hco/8/GRCh38#141217869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73457752-C-A

141217928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457798-G-T

http://identifiers.org/hco/8/GRCh38#141217929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73457799-C-A

141217929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73457799-C-T

141218077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: synonymous variant
orthologous variants: 73457934-A-G

141218151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: synonymous variant
orthologous variants: 73458008-G-A

141218151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: missense variant
orthologous variants: 73458008-G-T

http://identifiers.org/hco/8/GRCh38#141218287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73458141-C-A

141218287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: synonymous variant
orthologous variants: 73458141-C-T

141218323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: synonymous variant
orthologous variants: 73458177-G-A

141218323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: synonymous variant
orthologous variants: 73458177-G-T

141218587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: synonymous variant
orthologous variants: 73458438-G-A

141218587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: synonymous variant
orthologous variants: 73458438-G-T

141218613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: missense variant
orthologous variants: 73458464-T-G

141219140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73459005-G-A

141219140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73459005-G-C

141219140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73459005-G-T

141219329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73459163-G-A

http://identifiers.org/hco/8/GRCh38#141219334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73459168-C-A

141219412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73459220-A-G

http://identifiers.org/hco/8/GRCh38#141219777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73459521-C-A

141219777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 73459521-C-T

http://identifiers.org/hco/8/GRCh38#141219841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73459585-A-C

141219841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73459585-A-G

http://identifiers.org/hco/8/GRCh38#141219862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73459625-C-A

141220727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73460379-G-C

141220872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73460499-G-A

141221017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73460679-A-G

141221405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73461095-A-G

http://identifiers.org/hco/8/GRCh38#141221526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73461203-C-A

141221528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73461205-A-G

http://identifiers.org/hco/8/GRCh38#141221553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73461222-A-C

141221740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 73461398-G-A

141221740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 73461398-G-T

http://identifiers.org/hco/8/GRCh38#141221870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#73461465-C-A

141221870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, undefined
orthologous variants: 73461465-C-T

141222308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73461746-G-A

141222308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73461746-G-C

141222415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73461844-C-T

141222664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73461991-G-A

141222698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73462011-C-T

141222988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73462256-T-C

141223174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73462437-G-A

141223268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73462530-T-C

141227092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73465525-C-G

141227472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73465874-G-A

141227481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73465882-G-A

141227498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73465896-G-A

141235014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73467510-A-G

141235290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73467733-C-T

141235325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 73467764-G-A

141235397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73467810-T-A

141235397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73467810-T-C

141235704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73468063-G-A

141235713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73468072-T-C

141236821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73468813-T-G

141236905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73468863-A-G

141237191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73469138-G-A

141237245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73469174-T-C

141237490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73469332-C-G

141237490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73469332-C-T

141237495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73469337-T-A

141237512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, undefined
orthologous variants: 73469354-C-G

141237512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, undefined
orthologous variants: 73469354-C-T

141240110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73471422-T-C

141240167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73471460-A-G

141240180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73471473-C-T

141240244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73471534-C-T

141245322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73473783-C-T

141245420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73473879-T-C

141245679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73474097-C-T

141245842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73474340-A-G

141245867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73474365-A-G

141245940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73474433-C-T

141245974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73474465-G-T

141251633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73476348-C-G

141251641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73476354-T-C

141252207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73476884-T-C

141252268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron variant
orthologous variants: 73476943-G-A

141254206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73477511-G-A

141254336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73477644-T-C

141254626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73477922-T-A

141254627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 73477923-G-A

141254627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 73477923-G-T

http://identifiers.org/hco/8/GRCh38#141254707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73477988-C-A

141254799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73478031-C-G

141254931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73478126-T-C

141264563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73482910-G-A

141264563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73482910-G-C

http://identifiers.org/hco/8/GRCh38#141265145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73483313-C-A

141265262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73483426-T-C

141265399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73483570-G-A

141265607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73483777-C-T

141265916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73484046-C-T

141271652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73487376-C-T

141272195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73487634-C-G

141272292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73487689-A-T

141272370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73487779-T-C

141272887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73488419-A-G

141272994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73489012-T-C

141273559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73489527-A-G

141273705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73489672-T-C

http://identifiers.org/hco/8/GRCh38#141273759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73489721-A-C

141278742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73492724-G-C

141279097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73492948-G-A

141284666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73495471-T-C

141284892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73495632-T-A

141284904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73495644-C-T

141286129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73496646-G-A

141286381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73496929-T-A

141289206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73500947-G-A

141289206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73500947-G-C

141290403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73502583-C-T

141290639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73502864-A-T

141291203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73503043-T-C

http://identifiers.org/hco/8/GRCh38#141291474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73503465-A-C

http://identifiers.org/hco/8/GRCh38#141291482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73503473-C-A

141291486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73503477-T-C

141291486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73503477-T-G

141291488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73503479-G-T

141291599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73504052-G-A

141291600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73504053-T-C

141291713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73504170-G-C

141297264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73507291-G-A

http://identifiers.org/hco/8/GRCh38#141297362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73507356-C-A

141297362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73507356-C-G

141297362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73507356-C-T

141297784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73507745-G-A

141298321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73508429-G-A

http://identifiers.org/hco/8/GRCh38#141298427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73508491-C-A

141298671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73508667-A-T

141298672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73508668-G-C

141298696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73508687-G-A

141298696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73508687-G-C

141299542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73509496-G-A

141299634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73509604-C-T

141299635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73509605-C-T

141300191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73510138-C-T

141300403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73510321-G-T

141300458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73510370-A-G

141300849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73510710-C-G

141300863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73510724-G-T

141300901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73510757-C-T

141300969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73510827-G-A

http://identifiers.org/hco/8/GRCh38#141301050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73510879-C-A

141303527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73512709-C-T

http://identifiers.org/hco/8/GRCh38#141303546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73512728-A-C

141304653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73513850-A-T

http://identifiers.org/hco/8/GRCh38#141304736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73513955-C-A

141304738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73513957-C-T

141304739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73513958-G-A

141304873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73514100-T-C

141304888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73514115-T-G

141305299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73514935-C-G

141305302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73514938-G-C

141305458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515120-T-C

141305601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515265-G-A

141305627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515291-G-C

141305672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515332-A-T

http://identifiers.org/hco/8/GRCh38#141305770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#73515424-C-A

141305808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515460-T-C

141306033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515648-T-A

141306087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515695-C-G

141306113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515721-G-A

141306113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515721-G-C

141306168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73515779-C-G

141306502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73516126-T-A

141306502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73516126-T-G

141306573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73516198-T-C

141306746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73516355-G-A

141306822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73516419-C-G

141307025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73516601-T-G

141307364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73516944-A-G

141307514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73517022-G-A

141308016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73517318-G-A

141308016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73517318-G-C

141308016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73517318-G-T

http://identifiers.org/hco/8/GRCh38#141308088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73517335-C-A

141308088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73517335-C-T

http://identifiers.org/hco/8/GRCh38#141308165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29196
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#73517396-C-A