47935981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761042-A-G

47935989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761050-T-G

http://identifiers.org/hco/4/GRCh38#47936042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72761102-A-C

47936042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761102-A-G

47936045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761105-G-A

47936045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761105-G-T

47936050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761110-T-C

47936083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761136-T-C

47936150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761201-T-A

47936150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761201-T-G

http://identifiers.org/hco/4/GRCh38#47936155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72761206-A-C

47936203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761255-G-T

http://identifiers.org/hco/4/GRCh38#47936223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72761275-A-C

http://identifiers.org/hco/4/GRCh38#47936227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72761279-C-A

47936227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761279-C-T

47936306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761349-C-T

47936369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761407-A-G

47936385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761423-T-C

47936389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761427-G-T

47936390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761428-C-T

47936391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761429-A-G

47936392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761430-T-C

47936394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761437-T-A

47936394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761437-T-C

47936395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761438-C-T

47936398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72761441-T-C

47936433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72761476-G-A

47936433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72761476-G-T

47936448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72761491-C-T

47936573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72761616-A-G

http://identifiers.org/hco/4/GRCh38#47936736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72761779-A-C

47936736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72761779-A-G

47936988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72762031-A-G

47937021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72762064-C-T

47937279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72762322-T-A

47937387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72762430-G-A

47937387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72762430-G-T

47937447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72762490-G-A

47937447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 72762490-G-T

http://identifiers.org/hco/4/GRCh38#47937462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72762505-A-C

47937552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72762595-A-G

47937619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72762662-G-A

47937772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72762815-T-A

47937772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72762815-T-G

47937824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72762867-G-A

47937824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72762867-G-C

47937836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72762879-T-C

http://identifiers.org/hco/4/GRCh38#47937882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72762925-A-C

http://identifiers.org/hco/4/GRCh38#47937893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72762933-A-C

47937893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72762933-A-G

47937903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72762948-A-G

47937986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72763030-C-T

47938012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72763054-G-A

http://identifiers.org/hco/4/GRCh38#47938023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72763065-A-C

47939282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72764892-G-C

47939465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72765078-A-G

47939479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72765087-A-G

47939956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72765759-A-G

http://identifiers.org/hco/4/GRCh38#47940174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72765966-A-C

47940279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766067-C-G

47940279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766067-C-T

47940414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766203-T-A

http://identifiers.org/hco/4/GRCh38#47940423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72766212-C-A

47940423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766212-C-T

47940447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766242-T-A

47940491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766293-C-T

47940550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766354-C-T

47940558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766603-T-C

47940663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766701-T-A

47940698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766736-G-A

47940698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766736-G-T

http://identifiers.org/hco/4/GRCh38#47940707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72766743-C-A

47940707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766743-C-T

47940866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72766901-T-C

47940866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72766901-T-G

47940923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72766953-G-A

http://identifiers.org/hco/4/GRCh38#47940987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72767004-A-C

47940987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72767004-A-G

47941014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72767033-T-C

http://identifiers.org/hco/4/GRCh38#47941023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72767042-C-A

47941023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72767042-C-T

47941436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72767812-C-T

47941477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72767844-T-G

47941498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72767865-A-G

47941829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72767968-C-G

47941897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72768032-G-C

47941897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72768032-G-T

47942055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72768166-T-C

47942200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72768311-T-C

47942200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72768311-T-G

47942211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72768322-G-T

http://identifiers.org/hco/4/GRCh38#47942298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72768398-C-A

47942298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72768398-C-T

47942330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72768445-T-A

47942337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72768452-T-G

47942745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769095-G-A

47942754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769104-G-A

47942763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769121-G-T

47942806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769161-A-T

47942827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769182-T-A

47942827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769182-T-G

47942846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769200-T-A

47942846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769200-T-C

47942846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769200-T-G

http://identifiers.org/hco/4/GRCh38#47942850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72769204-A-C

47942850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769204-A-G

47942850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769204-A-T

http://identifiers.org/hco/4/GRCh38#47942856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72769210-C-A

47942856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769210-C-G

47942856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769210-C-T

47942999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72769341-A-G

http://identifiers.org/hco/4/GRCh38#47943098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72769422-C-A

47943098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72769422-C-T

http://identifiers.org/hco/4/GRCh38#47943192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72769515-A-C

47943362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769692-A-G

http://identifiers.org/hco/4/GRCh38#47943388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72769721-C-A

47943388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72769721-C-G

47943388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72769721-C-T

http://identifiers.org/hco/4/GRCh38#47943458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72769787-C-A

47943458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769787-C-G

47943510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72769847-G-T

47943641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72770534-A-G

47943690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72770589-A-G

47943746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72770643-A-T

47943824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72770723-T-G

47943842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72770741-C-G

47943847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72770754-C-T

47948217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72772252-G-A

47948874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72773171-T-A

47948936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72773230-T-C

47949285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72773554-C-T

47949697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72773952-T-G

47949701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72773956-A-G

47949701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72773956-A-T

47949935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72774166-C-T

47949956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72774178-T-C

47949956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72774178-T-G

http://identifiers.org/hco/4/GRCh38#47950619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72774451-A-C

47950621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72774453-T-A

47950621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72774453-T-C

47950628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72774461-G-A

47950628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72774461-G-T

47950702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72774531-G-A

47950765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72774587-T-C

47951155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775422-C-T

47951342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775500-A-G

47951342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775500-A-T

47951347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775505-G-A

47951347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775505-G-T

47951491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775634-A-T

47951531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775676-A-G

47951534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775679-T-C

47951534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775679-T-G

47951535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775680-T-G

47951554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775700-T-G

47951559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775705-C-T

http://identifiers.org/hco/4/GRCh38#47951573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72775719-C-A

47951588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72775734-A-G

47952010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72776136-C-T

47952633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72776405-A-G

http://identifiers.org/hco/4/GRCh38#47952720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72776492-C-A

47952770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72776538-T-C

47955546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72776583-G-A

47955546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72776583-G-C

47955712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72776732-T-A

47955804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72776818-C-T

47955838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72776853-A-G

47955919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72777059-C-T

47956140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72777259-G-A

47956140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72777259-G-C

47956343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72777471-G-A

47956343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72777471-G-T

47956589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72777740-G-T

47956633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72777795-T-A

47956785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72777917-G-A

47957832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72778933-G-A

47969065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72786714-A-G

47969070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72786719-T-A

47969230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72786879-C-T

47974269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72791527-A-T

http://identifiers.org/hco/4/GRCh38#47974688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72792094-A-C

47974757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72792148-T-C

47974781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72792178-T-G

47974833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72792229-G-A

47975481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72792846-T-A

http://identifiers.org/hco/4/GRCh38#47975482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72792847-C-A

47975569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72792923-T-G

47976353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72793638-A-G

47976417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72793691-T-C

47976419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72793693-A-T

47977163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72795184-C-T

47977274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72795292-A-G

47977385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72795377-T-A

47977385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72795377-T-G

47978374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72796440-C-T

47978429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72796469-T-C

47978435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72796475-A-G

47980089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72797823-T-A

47980249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72797971-T-C

47980341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72798062-T-C

47980348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72798069-T-C

47980368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72798089-A-G

47981031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72799470-G-C

47981168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72799611-T-C

47981228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72799684-T-A

47981352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72799805-G-A

47981416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72799866-C-T

http://identifiers.org/hco/4/GRCh38#47981469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72799920-C-A

47981469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72799920-C-T

47981723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72800178-G-A

47981759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72800213-C-G

47986796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72800873-G-C

47986816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72800893-G-C

47986910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72800989-G-C

47986930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801002-C-T

47986931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801003-T-C

47986931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801003-T-G

47987210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801220-A-G

47987356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801372-G-A

47987500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801514-G-A

47987571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801578-G-A

47987668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801675-G-C

47987951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801863-G-C

47988003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72801919-C-G

47988081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72802002-T-C

47988094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72802015-G-T

47988186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72802106-T-C

47988198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72802119-C-T

48013835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72802852-C-T

48014156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72803167-G-A

48014269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72803283-T-C

http://identifiers.org/hco/4/GRCh38#48014304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72803309-A-C

http://identifiers.org/hco/4/GRCh38#48014453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72803462-C-A

48015244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72804044-G-T

48015249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72804049-G-A

48015288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72804084-C-T

48015304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72804100-G-A

48016258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72804701-A-T

48016324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72804768-G-A

48016324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72804768-G-C

http://identifiers.org/hco/4/GRCh38#48016404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72804831-C-A

48016404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72804831-C-T

http://identifiers.org/hco/4/GRCh38#48016481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72804910-A-C

48016481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 72804910-A-G

48016498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72804927-G-A

48016498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72804927-G-T

48016589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72804996-G-T

48016612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72805016-G-C

48016612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72805016-G-T

http://identifiers.org/hco/4/GRCh38#48016619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72805022-C-A

48016619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72805022-C-T

http://identifiers.org/hco/4/GRCh38#48016620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72805023-C-A

48016620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72805023-C-T

48016623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72805026-G-T

48016627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72805030-G-A

48016627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72805030-G-T

http://identifiers.org/hco/4/GRCh38#48016628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72805031-C-A

48016628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72805031-C-T