9991190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129384093-A-G

9991271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129384038-G-T

9991322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129383991-A-G

9991333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129383950-G-T

http://identifiers.org/hco/12/GRCh38#9991473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129383815-A-C

9991473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129383815-A-G

9991505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129383784-C-T

http://identifiers.org/hco/12/GRCh38#9991569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129383683-A-C

9991636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129383622-A-G

9991660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129383599-A-G

9991833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129383446-A-G

9991862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129383405-G-T

9991980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129383292-T-G

http://identifiers.org/hco/12/GRCh38#9992001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129383277-C-A

http://identifiers.org/hco/12/GRCh38#9992073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129383209-C-A

9992759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382518-T-C

http://identifiers.org/hco/12/GRCh38#9992768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129382509-C-A

9992810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382492-A-G

9992860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382452-G-T

9992861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382451-A-T

http://identifiers.org/hco/12/GRCh38#9992959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129382372-C-A

9992973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382358-T-A

9992973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382358-T-C

9992990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382341-G-A

9992990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382341-G-C

9992990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382341-G-T

9993000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382333-T-C

9993025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382310-A-G

9993079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382274-T-C

9993126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382229-C-G

9993126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129382229-C-T

http://identifiers.org/hco/12/GRCh38#9993353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129382002-C-A

9993353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129382002-C-T

9993357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129382001-T-A

9993357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129382001-T-C

9993357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129382001-T-G

9993396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129381970-G-A

9993396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129381970-G-C

9993396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129381970-G-T

9993452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129381924-G-A

9993452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129381924-G-T

9993536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129381843-T-C

9993613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129381770-C-T

9994796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380933-A-G

9994816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380923-C-T

9994898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380834-G-T

9994934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380805-G-A

http://identifiers.org/hco/12/GRCh38#9995088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129380679-A-C

9995146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 129380622-T-C

http://identifiers.org/hco/12/GRCh38#9995271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129380497-A-C

9995271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129380497-A-G

9995271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129380497-A-T

9995291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380479-G-T

9995300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380472-A-G

9995304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380468-T-A

9995304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380468-T-C

9995352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380422-T-C

9995432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380342-T-A

9995435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380339-A-G

9995463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380315-A-G

9995474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380304-T-C

http://identifiers.org/hco/12/GRCh38#9995552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129380225-A-C

9995553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380224-T-A

9995553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380224-T-C

9995569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380208-A-G

http://identifiers.org/hco/12/GRCh38#9995582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129380195-A-C

9995582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380195-A-G

9995625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380155-T-C

9995656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380132-A-T

9995692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380110-G-A

9995692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380110-G-C

9995692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129380110-G-T

9995723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129380079-G-A

9995723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129380079-G-T

9995731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129380071-G-C

9995731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129380071-G-T

9995839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379904-G-A

9995839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379904-G-T

9995885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379837-G-A

9995989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379749-A-G

9995989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379749-A-T

9996053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379684-C-T

9996138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379581-A-G

9996260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379454-T-C

9996279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379436-G-A

9996485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379195-A-G

9996491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379184-C-T

9996622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379066-G-A

9996622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379066-G-T

9996623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379065-A-G

9996676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129379010-A-T

http://identifiers.org/hco/12/GRCh38#9996690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129378996-C-A

9996690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378996-C-G

9996812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378887-G-A

9996812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378887-G-T

9996877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: 129378823-G-A

9996877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: 129378823-G-C

9996907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: 129378793-C-G

9997101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378610-C-T

9997122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378592-G-A

9997141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378576-T-C

http://identifiers.org/hco/12/GRCh38#9997202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129378510-A-C

9997202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: 129378510-A-T

9997273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: 129378439-A-G

9997273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: 129378439-A-T

9997305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378406-A-G

9997334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378377-C-G

9997338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378373-G-A

9997338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378373-G-T

9997342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378369-T-C

http://identifiers.org/hco/12/GRCh38#9997345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129378366-C-A

9997354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378357-T-C

9997392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378319-T-C

9997392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129378319-T-G

9997751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129377642-A-T

9997786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129377603-A-G

9998044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129377363-G-A

http://identifiers.org/hco/12/GRCh38#9998151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129377245-C-A

9998151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129377245-C-T

9998189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129377206-C-T

9998203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129377192-T-C

http://identifiers.org/hco/12/GRCh38#9998231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129377169-C-A

9998268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129377130-G-T

http://identifiers.org/hco/12/GRCh38#9998345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129377053-C-A

9998345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: 129377053-C-G

9998346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant
orthologous variants: 129377052-C-G

9998363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 129377035-A-G

9998378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 129377023-C-T

9998415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129376987-C-T

9998784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129374886-C-G

http://identifiers.org/hco/12/GRCh38#9998928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129374743-C-A

9998977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129374693-G-A

9998977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129374693-G-T

9998988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129374682-A-G

9999025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129374651-G-T

http://identifiers.org/hco/12/GRCh38#9999153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129374520-A-C

9999153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374520-A-G

9999153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374520-A-T

9999169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374504-A-G

9999169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374504-A-T

9999199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374474-T-A

9999199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374474-T-C

9999199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374474-T-G

9999204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374470-T-C

9999259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374412-T-C

9999297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374374-G-A

9999297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129374374-G-T

http://identifiers.org/hco/12/GRCh38#9999384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129374293-C-A

9999384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129374293-C-G

9999384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129374293-C-T

http://identifiers.org/hco/12/GRCh38#9999439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129374235-C-A

9999439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129374235-C-T

9999441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129374233-T-G

10000023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129373585-C-T

10000626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129373131-C-T

10000753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 129372990-G-C

10000944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129372851-C-T

10001090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129372708-A-G

10001658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129372145-C-G

10001681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129372119-C-T

10001697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129372106-T-C

10001697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129372106-T-G

10001773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129372032-C-T

10001855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129371977-G-A

10001855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129371977-G-T

10001859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129371973-A-G

10001884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 129371941-T-C

10002306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129371856-T-C

10002309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129371853-T-C

10002332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129371830-T-C

10002337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129371825-G-C

10002970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129371215-A-G

10003013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129371193-G-A

10003273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129370641-G-A

10005862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129370178-A-T

10005964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129370102-T-A

http://identifiers.org/hco/12/GRCh38#10006062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129369986-A-C

10006080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129369970-C-T

10010150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362991-C-T

10010191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362958-G-C

10010236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362913-A-G

10010253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362900-A-G

10010432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362735-G-A

10010432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362735-G-T

10010528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362658-T-G

10010539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362646-A-G

10010539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362646-A-T

http://identifiers.org/hco/12/GRCh38#10010546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129362639-A-C

10010546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362639-A-G

10010546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362639-A-T

10010558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362635-T-C

http://identifiers.org/hco/12/GRCh38#10010561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129362632-A-C

10010561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362632-A-G

10010626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362567-A-G

10010626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron variant
orthologous variants: 129362567-A-T

10010799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 129362412-G-A

10010799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 129362412-G-T

http://identifiers.org/hco/12/GRCh38#10010822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129362389-C-A

10010822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 129362389-C-T

10010935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362279-T-C

10010937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362277-A-G

10010945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362269-G-A

10010945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362269-G-C

10010945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362269-G-T

10010955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362260-A-G

10010989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362238-A-G

10010989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362238-A-T

10011137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362104-T-A

10011203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362043-A-T

10011204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129362042-G-A

10011592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129360347-T-C

10011680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129360263-T-A

10011909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129360028-G-C

http://identifiers.org/hco/12/GRCh38#10012152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359850-C-A

10012180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359818-A-T

10012265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359764-T-A

10012508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359626-G-A

10012508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359626-G-C

http://identifiers.org/hco/12/GRCh38#10012661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359543-C-A

http://identifiers.org/hco/12/GRCh38#10012702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359503-C-A

http://identifiers.org/hco/12/GRCh38#10012725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359482-C-A

http://identifiers.org/hco/12/GRCh38#10012726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359481-C-A

10012726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359481-C-T

10012769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359452-T-C

10012789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 129359435-T-C

10012965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359270-G-T

10012999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359237-T-A

10012999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359237-T-G

http://identifiers.org/hco/12/GRCh38#10013007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359229-C-A

10013007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359229-C-G

10013007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359229-C-T

http://identifiers.org/hco/12/GRCh38#10013010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359226-A-C

10013010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359226-A-G

10013010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359226-A-T

http://identifiers.org/hco/12/GRCh38#10013025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359214-C-A

10013025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359214-C-T

10013044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359195-G-A

10013044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359195-G-T

http://identifiers.org/hco/12/GRCh38#10013071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359158-C-A

10013098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359131-C-T

10013106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359123-G-T

http://identifiers.org/hco/12/GRCh38#10013131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#129359100-C-A

10013131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359100-C-T

10013226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129359007-A-G

10013324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129358912-A-G

10013374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: intron_variant, undefined
orthologous variants: 129358861-G-A

10013404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24356
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 129358828-G-A