159169423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8046106-G-A

159169423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8046106-G-T

http://identifiers.org/hco/6/GRCh38#159169430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8046099-C-A

159169455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8046074-G-T

159169489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8046051-A-G

159169499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8046041-G-A

159169499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8046041-G-T

http://identifiers.org/hco/6/GRCh38#159169570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8045974-C-A

159169570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8045974-C-G

159169570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8045974-C-T

http://identifiers.org/hco/6/GRCh38#159169576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8045968-C-A

159169576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8045968-C-T

http://identifiers.org/hco/6/GRCh38#159169593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8045951-C-A

159169593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8045951-C-G

159169593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8045951-C-T

http://identifiers.org/hco/6/GRCh38#159169620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8045924-C-A

159169620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8045924-C-G

159169620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8045924-C-T

http://identifiers.org/hco/6/GRCh38#159169678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8045875-C-A

159169678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 8045875-C-T

159169707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 8045846-T-A

159169707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 8045846-T-C

159169707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 8045846-T-G

159169809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8045730-A-G

159169815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8045724-T-A

159169844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8045682-C-T

http://identifiers.org/hco/6/GRCh38#159170102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8045443-C-A

159170102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8045443-C-T

159170507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8045138-G-A

159171110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8044522-T-A

159171110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8044522-T-C

159171125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8044508-G-T

http://identifiers.org/hco/6/GRCh38#159171137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8044492-C-A

159173355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8041873-C-T

159173648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8041601-A-G

http://identifiers.org/hco/6/GRCh38#159173844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8041399-C-A

159173873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8041365-C-G

159173873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8041365-C-T

159173994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8041252-G-C

159174057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8041202-G-T

159174156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8041090-C-G

159174553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, undefined
orthologous variants: 8040780-G-A

159174628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, undefined
orthologous variants: 8040748-T-G

http://identifiers.org/hco/6/GRCh38#159174791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8040619-C-A

159174791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8040619-C-T

159174857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8040551-T-A

159175126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8040357-C-G

159175317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8040201-T-C

159184541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8037978-C-G

159184544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8037975-G-T

159184575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8037960-A-G

159184638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8037896-A-G

159184772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8037748-G-T

159184833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8037686-T-C

159185293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8037243-A-G

159185593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8036987-C-G

159185700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8036880-C-T

http://identifiers.org/hco/6/GRCh38#159185751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8036865-C-A

159186199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8036062-C-T

159186204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8036057-T-G

http://identifiers.org/hco/6/GRCh38#159186568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8035788-A-C

159186607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8035751-G-A

159187206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8035211-T-G

159187214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8035203-A-G

159187290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8035154-G-A

159187578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8034673-C-T

159187599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8034664-G-A

159187602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8034661-G-A

159187708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8034437-G-C

159187713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8034432-T-C

159188144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8033564-T-A

http://identifiers.org/hco/6/GRCh38#159188154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8033554-A-C

http://identifiers.org/hco/6/GRCh38#159188222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8033510-A-C

159189134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8033219-A-T

159189450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8032873-T-C

159189997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8030920-T-C

http://identifiers.org/hco/6/GRCh38#159190065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8030876-C-A

159190117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8030823-A-G

159190132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8030808-C-T

159190224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8030712-G-C

159190224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8030712-G-T

159190434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8030525-C-T

159190728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8030263-A-G

159191567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8029826-T-C

159192356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8028995-T-C

159192386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8028969-A-G

159192543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8028842-A-T

159192768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8028645-C-T

159192865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8028551-T-A

159192981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8028440-G-A

159193007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8028419-T-C

159193299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8027965-C-T

159193738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8027596-C-G

159194057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8027263-A-G

159194433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8026898-G-T

159194558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8026586-A-G

159194807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8026369-A-T

159196316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8024981-T-C

159196470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8024836-C-T

159197027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8024253-G-A

159197216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8024061-C-T

http://identifiers.org/hco/6/GRCh38#159197364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8023917-A-C

159197364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8023917-A-G

159197369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8023912-T-G

http://identifiers.org/hco/6/GRCh38#159197385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8023897-C-A

159197385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8023897-C-T

159197390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8023892-T-A

159197399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8023883-G-T

159197977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8023319-C-T

159198118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8022202-G-A

159198465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8021932-C-G

159198558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8021866-G-A

159198619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8021813-G-A

159198713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8021686-A-G

159198765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8021632-T-C

159199080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8021339-T-A

http://identifiers.org/hco/6/GRCh38#159199112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8021307-C-A

159199112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8021307-C-G

159199112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8021307-C-T

159199173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8021247-C-T

159199435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8020990-G-T

159199554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8020888-T-C

159199851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8020603-T-G

159200055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, missense_variant
orthologous variants: 8020425-C-T

159200114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8020373-G-A

159200114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8020373-G-T

159200122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8020365-T-C

159200122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8020365-T-G

159200247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8020054-G-A

159200423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8019883-A-G

http://identifiers.org/hco/6/GRCh38#159200467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8019839-C-A

159200467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8019839-C-T

159200523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, stop_gained
orthologous variants: 8019783-G-A

159200601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8019711-G-A

159200601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8019711-G-T

159200683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8019630-G-A

159200683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8019630-G-T

159201421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8018973-G-A

159201556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8018829-G-A

http://identifiers.org/hco/6/GRCh38#159201741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8017184-C-A

159201760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8017165-A-G

159201793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8017132-G-A

http://identifiers.org/hco/6/GRCh38#159201817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8017108-A-C

159201931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8017016-C-T

159202053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8016863-T-C

159202095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8016822-C-T

159202381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8016559-C-G

159202409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8016530-G-A

159202667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8016274-T-C

http://identifiers.org/hco/6/GRCh38#159203131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8015803-C-A

159203543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8015453-G-A

159203585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8015434-G-A

159203607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8015412-T-A

159204329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8014830-C-T

159204426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8014769-C-T

159204441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8014755-C-T

159204585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8014637-A-T

159204610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8014620-C-T

http://identifiers.org/hco/6/GRCh38#159204820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8014429-A-C

159207362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8013835-C-T

http://identifiers.org/hco/6/GRCh38#159207481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8013751-C-A

159207640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8013602-T-C

http://identifiers.org/hco/6/GRCh38#159207642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8013600-A-C

159207675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8013576-T-G

159208219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8013068-G-A

159208230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8013057-A-G

159208260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8013027-T-A

159208525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8012836-C-T

159208564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8012795-C-T

159208700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8012681-G-A

159209229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8012461-T-A

159209266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8012426-G-C

159209445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8012291-A-G

159209468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8012269-G-T

159209850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8011921-A-G

159210172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8011547-G-A

159210193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8011530-C-T

159210202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8011521-A-G

159210283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8011442-G-A

159210301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8011424-C-T

159210361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8011364-T-C

159210615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8010975-A-G

159210631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8010959-G-T

159212038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8010557-C-T

159212089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8010511-T-A

159212434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8010166-G-A

http://identifiers.org/hco/6/GRCh38#159212663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8009963-C-A

159213199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8009576-G-A

159213199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8009576-G-C

159213399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8009387-T-C

159213514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8009287-G-A

159213666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8009168-G-T

159213819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8009037-G-T

159213989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008900-A-T

159214261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008657-T-C

159214309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008612-C-G

159214360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008573-A-T

159214575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008361-T-G

159214606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008330-T-G

159214881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008084-G-T

159214902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008071-G-A

159214905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008070-G-A

http://identifiers.org/hco/6/GRCh38#159214907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8008068-C-A

159214907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8008068-C-G

159215058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 8007917-C-T

159215061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 8007914-G-A

159215207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8007780-A-G

159215237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8007750-T-A

159215237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8007750-T-C

159216509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006788-G-A

159216841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006521-T-A

159216841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006521-T-C

159217007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006382-C-T

159217011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006378-G-C

159217075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006286-G-A

159217146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006219-G-T

159217147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006218-G-A

159217147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006218-G-C

http://identifiers.org/hco/6/GRCh38#159217333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8006052-C-A

159217333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8006052-C-G

159217694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, undefined
orthologous variants: 8005728-T-C

159217895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8005554-C-G

159217980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8005477-T-G

159218031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8005410-C-T

159218061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8005382-C-T

159218164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8005302-A-G

http://identifiers.org/hco/6/GRCh38#159218176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8005290-C-A

159218288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 8005186-G-A

159218390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8005086-C-G

159218475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8005036-G-A

159218475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8005036-G-T

159218505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8005032-G-C

159218505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8005032-G-T

159218604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8004933-A-G

159218673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8004859-G-A

159218839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8004754-G-A

159219028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8004564-G-C

159221699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8003173-A-G

159221699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8003173-A-T

159221725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8003144-A-G

http://identifiers.org/hco/6/GRCh38#159221757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8003117-C-A

159221757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8003117-C-T

http://identifiers.org/hco/6/GRCh38#159221785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8003073-C-A

159221785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8003073-C-T

159221787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8003071-T-A

159221787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8003071-T-G

159221912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8002964-G-T

http://identifiers.org/hco/6/GRCh38#159222155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8002744-C-A

159222165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8002734-G-A

159222338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8002151-T-C

159222351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8002142-A-G

159222381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8002102-T-C

159222421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8002067-A-G

159222553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8001956-G-A

http://identifiers.org/hco/6/GRCh38#159222674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8001832-A-C

159222810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8001693-G-A

159222872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8001631-G-A

159222920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

159222929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/6/GRCh38#159223380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8001449-A-C

http://identifiers.org/hco/6/GRCh38#159223421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8001408-A-C

159223537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8001309-A-G

159223681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8001162-A-G

http://identifiers.org/hco/6/GRCh38#159223700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8001143-C-A

http://identifiers.org/hco/6/GRCh38#159223709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#8001099-C-A

159223709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8001099-C-T

159223774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8000972-G-A

159223774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8000972-G-T

159223798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8000916-C-T

159224658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8000022-C-T

159224716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7999963-T-C

159224771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7999908-T-C

159225049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7999539-G-A

159225390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7999211-A-G

http://identifiers.org/hco/6/GRCh38#159225450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7999153-A-C

159225450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7999153-A-T

159225455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7999148-T-C

159225455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7999148-T-G

159225635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7998961-A-G

159225668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7998928-G-A

http://identifiers.org/hco/6/GRCh38#159225713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7998883-C-A

159225713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7998883-C-G

159225713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7998883-C-T

http://identifiers.org/hco/6/GRCh38#159225788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7998794-C-A

159225788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7998794-C-G

http://identifiers.org/hco/6/GRCh38#159225817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7998700-C-A

159225817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7998700-C-T

159225830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7998643-T-C

159225830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7998643-T-G

http://identifiers.org/hco/6/GRCh38#159225852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7998606-A-C

159225856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7998600-T-G

http://identifiers.org/hco/6/GRCh38#159225868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7998588-C-A

159225874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7998582-G-A

159225885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7998567-G-T

159226288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7998011-T-C

159226464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7997593-A-G

159226652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7997416-T-C

http://identifiers.org/hco/6/GRCh38#159226678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7997375-C-A

159226678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7997375-C-T

159226868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7997202-A-G

159227162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7996921-A-G

159227208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7996875-T-C

159227435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7996662-A-T

159227586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7996510-T-C

159227652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7996456-T-C

159229214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994953-T-C

159229286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994889-A-G

159229286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994889-A-T

159229392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994814-C-G

159229432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994776-G-C

159229492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994709-A-T

159229519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994682-G-A

159229557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994645-T-C

159229581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994621-G-T

159229646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994564-A-G

159229753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994458-G-A

159229829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, missense_variant
orthologous variants: 7994382-T-A

http://identifiers.org/hco/6/GRCh38#159230040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7994171-C-A

159230040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994171-C-T

159230042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994169-T-G

159230072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994125-G-A

159230072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994125-G-T

159230075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994122-T-A

159230119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994078-G-A

159230119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994078-G-C

159230119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994078-G-T

159230190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7994008-T-C

159230619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7993784-T-C

159230690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7993714-G-T

159230763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7993642-A-G

159230925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7993499-A-G

159231093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7993367-G-A

159231097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7993363-C-T

159231938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7992567-G-A

159231968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7992537-G-A

159231968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7992537-G-C

159232057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7992466-T-C

159232059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7992464-A-G

159232137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7992389-G-C

http://identifiers.org/hco/6/GRCh38#159232271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7992255-C-A

159232271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7992255-C-G

159232271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7992255-C-T

159232313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7992213-G-T

159232487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7992084-C-T

159232504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7992067-C-G

http://identifiers.org/hco/6/GRCh38#159232574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7991973-C-A

159232648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991896-C-T

159232660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991884-C-G

159232660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991884-C-T

http://identifiers.org/hco/6/GRCh38#159232759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7991821-C-A

159232759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991821-C-T

159232770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991810-C-T

159232819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991773-T-C

159232879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991713-C-G

159232879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991713-C-T

159232888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991704-C-T

http://identifiers.org/hco/6/GRCh38#159233008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7991584-A-C

159233008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991584-A-G

159233045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991547-C-G

http://identifiers.org/hco/6/GRCh38#159233057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7991535-C-A

159233057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991535-C-T

http://identifiers.org/hco/6/GRCh38#159233114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7991478-C-A

http://identifiers.org/hco/6/GRCh38#159233162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7991430-C-A

159233162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991430-C-T

159233174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991418-A-G

http://identifiers.org/hco/6/GRCh38#159233210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7991382-C-A

159233272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991320-T-C

159233331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991261-G-A

159233338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991257-C-T

159233386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991209-G-A

159233386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991209-G-T

http://identifiers.org/hco/6/GRCh38#159233399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7991208-C-A

159233400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991207-A-G

159233576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991061-A-G

159233602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7991041-G-A

159233602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7991041-G-T

159233677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous_variant, undefined
orthologous variants: 7991002-T-A

159233701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990978-G-A

159233701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990978-G-T

http://identifiers.org/hco/6/GRCh38#159233897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7990791-C-A

159233897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990791-C-T

159233905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990783-T-A

159233905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990783-T-G

http://identifiers.org/hco/6/GRCh38#159233943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7990745-C-A

159233943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990745-C-G

159234039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: stop gained
orthologous variants: 7990637-C-G

159234039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990637-C-T

http://identifiers.org/hco/6/GRCh38#159234137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7990545-C-A

159234137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990545-C-G

159234137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990545-C-T

159234228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990461-C-T

http://identifiers.org/hco/6/GRCh38#159234267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7990433-C-A

159234267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990433-C-T

159234304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7990396-C-T

159234310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: 7990390-T-A

159234326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990374-G-T

159234375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990325-G-A

159234375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990325-G-T

159234441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7990262-C-G

http://identifiers.org/hco/6/GRCh38#159234571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7990111-C-A

159234571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7990111-C-G

http://identifiers.org/hco/6/GRCh38#159234581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7990095-C-A

159234581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7990095-C-T

http://identifiers.org/hco/6/GRCh38#159234613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7990072-C-A

159235442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7989261-C-T

159235539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7989170-A-T

159235795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7988968-T-G

159235968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7988821-T-G

159236176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7988632-T-A

159236210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 7988591-T-C

159236239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7988562-A-G

159236333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7988468-A-G

159236372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7988434-A-G

http://identifiers.org/hco/6/GRCh38#159236425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7987947-C-A

159236425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7987947-C-T

159236628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7987728-T-C

159236688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7987685-T-A

159236688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7987685-T-C

159236688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7987685-T-G

159236796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7987226-T-A

159236867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7987152-T-C

159237385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7986482-T-C

159237398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7986469-T-C

159237628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7986235-G-C

159237628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7986235-G-T

159237646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7986212-A-G

http://identifiers.org/hco/6/GRCh38#159238448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7985434-A-C

159238448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985434-A-G

159238448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985434-A-T

159238458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985424-T-C

159238458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985424-T-G

http://identifiers.org/hco/6/GRCh38#159238459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7985423-C-A

159238459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985423-C-G

159238459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985423-C-T

159238462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985420-T-C

159238462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985420-T-G

159238473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985412-G-A

159238473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985412-G-T

159238474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985411-G-A

159238474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985411-G-C

159238474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985411-G-T

http://identifiers.org/hco/6/GRCh38#159238544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7985341-A-C

159238544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985341-A-G

159238544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985341-A-T

159238569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7985314-C-T

http://identifiers.org/hco/6/GRCh38#159238697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7985187-C-A

159238697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985187-C-G

159238699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985185-T-A

159238699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985185-T-G

159238703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985181-G-T

http://identifiers.org/hco/6/GRCh38#159238734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7985157-C-A

159238734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985157-C-T

159238817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7985075-C-G

159239156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7984685-A-G

159239377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7984400-G-T

http://identifiers.org/hco/6/GRCh38#159239406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7984348-C-A

159239423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7984331-A-G

http://identifiers.org/hco/6/GRCh38#159239443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7984311-C-A

http://identifiers.org/hco/6/GRCh38#159239491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7984263-A-C

159239491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7984263-A-G

http://identifiers.org/hco/6/GRCh38#159239753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7983995-A-C

http://identifiers.org/hco/6/GRCh38#159239809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7983939-C-A

159239933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7983812-A-G

159239948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7983797-G-A

159239948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7983797-G-C

159239948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7983797-G-T

159240044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7983705-G-A

159240044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7983705-G-T

159240144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7983646-G-A

159240493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7983295-G-C

http://identifiers.org/hco/6/GRCh38#159240600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7983187-C-A

159240600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7983187-C-T

159240726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7983098-A-G

159240726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7983098-A-T

http://identifiers.org/hco/6/GRCh38#159240836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7983022-C-A

159240962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7982915-G-A

159240972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7982905-A-G

http://identifiers.org/hco/6/GRCh38#159241257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7982402-A-C

159241272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7982360-G-A

159241272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7982360-G-C

159241272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7982360-G-T

159241288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7982341-T-G

159241515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7982111-G-A

159241685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7981946-C-T

http://identifiers.org/hco/6/GRCh38#159243060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7980529-C-A

159243142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7980457-G-A

http://identifiers.org/hco/6/GRCh38#159243149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7980450-C-A

http://identifiers.org/hco/6/GRCh38#159243240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7980362-C-A

159243258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7980346-G-T

159243271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7980333-G-T

159243336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7980267-G-A

159243523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7980068-A-G

159243636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7979941-C-T

http://identifiers.org/hco/6/GRCh38#159243637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7979940-A-C

159243637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7979940-A-G

159243755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7979843-T-A

159243928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7979678-G-C

159244054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7979553-A-T

159244237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7979286-C-T

159244466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7979039-G-C

159244522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7978995-A-G

159244522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7978995-A-T

159244554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7978963-A-G

http://identifiers.org/hco/6/GRCh38#159244692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7978751-A-C

http://identifiers.org/hco/6/GRCh38#159246335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7977869-C-A

159246364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977840-T-C

159246364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977840-T-G

159246396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977807-T-C

159246522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977703-G-A

159246522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977703-G-T

159246558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977664-T-G

159246793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977464-T-C

159246794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977463-T-C

159246794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977463-T-G

http://identifiers.org/hco/6/GRCh38#159246804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7977453-C-A

http://identifiers.org/hco/6/GRCh38#159246825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7977434-C-A

159246825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977434-C-T

http://identifiers.org/hco/6/GRCh38#159246977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7977284-C-A

159246983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977278-T-C

159247373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977098-C-T

159247395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977076-T-C

159247421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7977048-T-C

159247846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7976942-A-T

159247914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7976876-T-C

http://identifiers.org/hco/6/GRCh38#159247927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7976865-C-A

159247927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7976865-C-G

159247928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7976864-C-T

http://identifiers.org/hco/6/GRCh38#159248195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7976620-A-C

159248215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7976603-T-C

159248512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7976170-G-A

159248528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7976154-T-C

159248548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7976118-C-T

159248555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7976111-C-T

http://identifiers.org/hco/6/GRCh38#159248694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7975977-C-A

159248920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975345-T-A

159248920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975345-T-C

159248926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975339-T-A

159248926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975339-T-C

http://identifiers.org/hco/6/GRCh38#159248945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7975319-C-A

159248945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975319-C-G

159248945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975319-C-T

159248982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975285-A-G

159248982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975285-A-T

159249089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7975181-A-G

http://identifiers.org/hco/6/GRCh38#159249185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7975085-A-C

159249185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975085-A-G

159249194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975076-G-A

159249208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975062-A-G

159249228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975045-T-C

http://identifiers.org/hco/6/GRCh38#159249267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7975019-C-A

159249267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7975019-C-G

159249330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7974953-G-A

159249372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7974918-A-G

159249752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7974211-T-C

159249757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7974202-C-T

159249803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7974154-G-A

159249900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7974057-C-T

159250079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7973885-A-T

159250080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7973884-T-A

159250787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7973405-T-A

159250787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7973405-T-G

159251156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7972721-T-C

159251215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7972667-G-A

159251215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7972667-G-T

159251337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7972545-G-A

159251340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7972542-C-T

159251388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7972494-G-A

159251427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7972455-C-T

159251481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7972401-T-A

159251603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7972295-A-T

159251625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7972274-G-T

159251833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7972087-T-C

http://identifiers.org/hco/6/GRCh38#159251905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7972016-C-A

159251934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7971989-A-G

159251963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7971970-C-G

159251968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7971965-T-C

159252105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7971857-G-A

http://identifiers.org/hco/6/GRCh38#159252288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7971681-C-A

159252343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7971636-T-C

159252598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7971374-G-A

159252598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7971374-G-C

159252730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7971237-C-G

159256180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7970023-G-A

159256198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7970005-T-C

159256256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969939-G-A

159256309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969882-G-A

159256367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969828-C-T

159256428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969763-T-C

159256472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969726-T-C

159256479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969327-T-G

159256505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969301-T-C

http://identifiers.org/hco/6/GRCh38#159256635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7969170-C-A

159256635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969170-C-T

http://identifiers.org/hco/6/GRCh38#159256644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7969161-A-C

159256644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969161-A-G

159256691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969111-T-G

159256693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969109-G-C

159256693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969109-G-T

159256741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7969067-T-C

159257048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7968785-T-C

159257413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7968414-G-A

159257469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7968343-G-T

159257659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7968189-C-T

159257905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7967968-C-T

159257966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7967916-A-T

159257980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7967900-A-T

159258011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7967869-T-G

159258191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7967692-C-T

159258259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7967612-T-C

159258274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7967597-T-C

http://identifiers.org/hco/6/GRCh38#159258324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7967549-C-A

159258360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7967521-G-A

159259589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7967059-T-G

159259669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7966962-A-T

159259734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7966902-G-C

http://identifiers.org/hco/6/GRCh38#159260137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7966553-A-C

159260308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7966435-T-C

159260328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7966415-T-G

http://identifiers.org/hco/6/GRCh38#159260477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7966203-C-A

http://identifiers.org/hco/6/GRCh38#159261054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7965683-C-A

http://identifiers.org/hco/6/GRCh38#159261067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7965670-C-A

159261067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7965670-C-T

159261133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7965531-T-C

159261230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7965434-G-A

159263951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7963673-G-A

159264042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7963574-T-A

http://identifiers.org/hco/6/GRCh38#159264420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7963133-C-A

159264420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7963133-C-T

159264641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7962924-G-A

http://identifiers.org/hco/6/GRCh38#159264755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7961962-C-A

159264873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961845-T-C

159264880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961838-A-G

http://identifiers.org/hco/6/GRCh38#159264919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7961799-A-C

159264992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7961735-G-A

159265056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961664-T-C

159265059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961661-A-G

159265138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961587-T-A

159265145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961580-G-A

159265145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961580-G-C

159265145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961580-G-T

159265494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961254-G-A

159265494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7961254-G-T

http://identifiers.org/hco/6/GRCh38#159265949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7960727-C-A

159266040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7960657-C-G

159266197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7960500-C-G

159266333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7960379-G-A

159267161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7960233-G-A

159267220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7960183-C-G

159267220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7960183-C-T

159267236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, undefined
orthologous variants: 7960167-T-C

159267293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, undefined
orthologous variants: 7960093-G-A

159267324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, undefined
orthologous variants: 7960063-T-C

159267382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, undefined
orthologous variants: 7960006-C-T

159267655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959765-A-G

159267799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 7959625-T-A

159267799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 7959625-T-C

159267945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959481-T-A

159267955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959471-T-C

159267960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959467-G-A

159267960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959467-G-T

159267961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959466-G-A

159267961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959466-G-T

159268039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959389-T-C

159268046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959382-A-T

159268076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959354-G-C

159268076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7959354-G-T

159270468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7958758-G-C

159270651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7958596-G-T

159270740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7958523-T-C

159271188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7958276-T-C

159271188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7958276-T-G

159271202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7958262-A-G

159271250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7958222-A-G

159271262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7958209-G-A

159271262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: intron variant
orthologous variants: 7958209-G-T

159271335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: missense variant
orthologous variants: 7958152-C-T

159271529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957958-G-A

159271529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957958-G-T

159271570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957917-G-A

159271570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957917-G-C

159271570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957917-G-T

http://identifiers.org/hco/6/GRCh38#159271571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7957916-A-C

159271571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957916-A-G

159271571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957916-A-T

http://identifiers.org/hco/6/GRCh38#159271574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7957914-C-A

159271574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957914-C-G

159271574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957914-C-T

159271603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957887-C-T

159271648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957842-G-A

159271679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957812-T-A

159271684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957807-T-C

http://identifiers.org/hco/6/GRCh38#159271715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7957778-C-A

http://identifiers.org/hco/6/GRCh38#159271728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7957765-C-A

http://identifiers.org/hco/6/GRCh38#159271823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#7957676-C-A

159271823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957676-C-T

159271882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957627-G-C

159271918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957591-C-T

159271976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957540-G-T

159272031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21184
most severe consequence: 3 prime UTR variant
orthologous variants: 7957473-G-A