43166628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459850-A-G

43166634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459856-G-A

43166634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459856-G-T

43166641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459863-T-C

http://identifiers.org/hco/22/GRCh38#43166674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83459889-C-A

43166674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459889-C-T

43166675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459890-A-G

43166675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459890-A-T

http://identifiers.org/hco/22/GRCh38#43166698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83459918-C-A

43166698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459918-C-T

43166806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459986-G-A

43166806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83459986-G-T

http://identifiers.org/hco/22/GRCh38#43166861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460038-A-C

http://identifiers.org/hco/22/GRCh38#43166887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460063-C-A

http://identifiers.org/hco/22/GRCh38#43166955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460111-C-A

43166955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460111-C-G

http://identifiers.org/hco/22/GRCh38#43166977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460133-C-A

http://identifiers.org/hco/22/GRCh38#43166978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460134-A-C

43167123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460281-T-C

43167123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460281-T-G

43167263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460437-G-A

43167263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460437-G-T

43167265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460439-G-A

43167265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460439-G-C

43167265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460439-G-T

43167270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460444-G-A

43167270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460444-G-T

43167318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460463-A-G

43167322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460467-T-C

43167337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460482-G-T

43167413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460542-A-G

43167415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460544-T-C

http://identifiers.org/hco/22/GRCh38#43167464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460592-C-A

43167483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460594-T-C

http://identifiers.org/hco/22/GRCh38#43167510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460622-C-A

43167510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460622-C-T

43167579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460688-C-T

43167603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460713-G-A

43167603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460713-G-T

http://identifiers.org/hco/22/GRCh38#43167615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460725-C-A

43167615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460725-C-T

http://identifiers.org/hco/22/GRCh38#43167698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460763-C-A

43167698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460763-C-T

http://identifiers.org/hco/22/GRCh38#43167785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83460855-C-A

43167785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460855-C-T

43167838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460899-T-C

43167855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460915-G-A

43167867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460926-T-A

43167867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460926-T-C

43167878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83460937-G-T

43167964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83461040-G-T

43167981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83461062-A-G

43167992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83461073-T-C

http://identifiers.org/hco/22/GRCh38#43167998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83461079-C-A

43167998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83461079-C-G

43167998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83461079-C-T

43168113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83461203-G-A

43168113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83461203-G-C

http://identifiers.org/hco/22/GRCh38#43168179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83461263-C-A

43168268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461339-A-G

43168282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461353-A-G

http://identifiers.org/hco/22/GRCh38#43168306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83461374-C-A

http://identifiers.org/hco/22/GRCh38#43168420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83461471-C-A

43168549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461531-G-A

43168559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461541-C-T

43168666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461654-T-G

http://identifiers.org/hco/22/GRCh38#43168671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83461659-C-A

43168671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461659-C-G

43168681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461707-G-C

43168723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461892-G-T

43168728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461897-G-A

43168737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461905-T-G

43168744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461912-T-C

http://identifiers.org/hco/22/GRCh38#43168750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83461918-C-A

43168750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461918-C-T

http://identifiers.org/hco/22/GRCh38#43168764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83461939-C-A

43168764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461939-C-T

43168802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83461976-G-A

43168880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83462054-G-T

43168883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83462057-C-G

43168917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83462091-G-T

43168964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462141-G-A

43168964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462141-G-T

http://identifiers.org/hco/22/GRCh38#43168985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83462162-C-A

43168985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462162-C-T

43169005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462182-G-A

43169005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462182-G-T

43169048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462223-A-G

http://identifiers.org/hco/22/GRCh38#43169050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83462227-C-A

43169265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462626-G-A

43169279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462641-G-A

http://identifiers.org/hco/22/GRCh38#43169309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83462683-C-A

43169355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462748-C-T

43169372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462766-T-C

43169372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462766-T-G

43169399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83462773-T-C

http://identifiers.org/hco/22/GRCh38#43169446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83462809-C-A

43169595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83462930-C-T

43169733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463030-A-G

43169798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463077-C-G

43169813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463092-G-A

43169813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463092-G-C

43169813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463092-G-T

43169820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463098-G-A

43169823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463101-C-T

43169864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463140-C-G

43169864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463140-C-T

43169871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463147-G-C

43169871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463147-G-T

http://identifiers.org/hco/22/GRCh38#43169919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83463185-C-A

43169919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463185-C-T

http://identifiers.org/hco/22/GRCh38#43169960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83463226-C-A

43169974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463240-G-A

http://identifiers.org/hco/22/GRCh38#43169990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83463247-C-A

43169990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463247-C-T

43170041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463278-G-A

43170041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463278-G-T

43170069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463302-G-A

http://identifiers.org/hco/22/GRCh38#43170114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83463340-C-A

43170114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463340-C-G

43170114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463340-C-T

http://identifiers.org/hco/22/GRCh38#43170125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83463351-C-A

http://identifiers.org/hco/22/GRCh38#43170126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83463352-C-A

43170126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463352-C-T

http://identifiers.org/hco/22/GRCh38#43170159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83463385-C-A

43170159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463385-C-T

http://identifiers.org/hco/22/GRCh38#43170162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83463388-A-C

43170173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463397-C-T

43170175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83463399-C-G

http://identifiers.org/hco/22/GRCh38#43171795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83464245-C-A

43171795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464245-C-T

43171798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464248-T-C

http://identifiers.org/hco/22/GRCh38#43171800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83464250-C-A

43171800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464250-C-T

43171931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464381-T-A

43171931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464381-T-G

http://identifiers.org/hco/22/GRCh38#43171969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83464392-C-A

43171993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464400-T-C

43172026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464419-G-A

43172026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464419-G-T

43172032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464425-G-A

43172083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464476-G-A

http://identifiers.org/hco/22/GRCh38#43172090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83464483-A-C

http://identifiers.org/hco/22/GRCh38#43172270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83464602-C-A

43172270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464602-C-T

43172323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464642-A-G

43172357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464655-G-A

43172357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464655-G-C

43172371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464666-C-T

http://identifiers.org/hco/22/GRCh38#43172383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83464678-C-A

43172592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464895-C-G

43172610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464920-C-T

43172612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464922-G-A

43172612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464922-G-T

http://identifiers.org/hco/22/GRCh38#43172636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83464975-C-A

43172636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464975-C-G

43172636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464975-C-T

43172645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464994-G-T

43172646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83464995-G-T

43173699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83465846-G-A

43173699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83465846-G-T

43173704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83465851-G-A

43173704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83465851-G-T

43173882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83466022-G-A

43173882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83466022-G-T

http://identifiers.org/hco/22/GRCh38#43173917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83466056-C-A

43173940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83466081-G-A

43173940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83466081-G-T

http://identifiers.org/hco/22/GRCh38#43174257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83466294-C-A

43174257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: missense variant
orthologous variants: 83466294-C-T

43174470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83466528-A-G

43174472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83466530-G-A

43174537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83466585-G-A

43174537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83466585-G-C

43174540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83466588-G-A

http://identifiers.org/hco/22/GRCh38#43174602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83466650-C-A

43174602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83466650-C-G

43174602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83466650-C-T

http://identifiers.org/hco/22/GRCh38#43174606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83466654-C-A

43174606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83466654-C-G

43174606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83466654-C-T

http://identifiers.org/hco/22/GRCh38#43174645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83466688-C-A

43174645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83466688-C-G

43174645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83466688-C-T

43174666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83466705-G-A

43174666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83466705-G-T

http://identifiers.org/hco/22/GRCh38#43174681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83466709-C-A

43174681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83466709-C-T

43174750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83466754-T-C

43174986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83466950-C-T

43175055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83468172-A-G

43175056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83468173-G-T

http://identifiers.org/hco/22/GRCh38#43175186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83468319-C-A

43175186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83468319-C-G

43175186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83468319-C-T

43175206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83468341-G-T

http://identifiers.org/hco/22/GRCh38#43175243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83468374-A-C

43175243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83468374-A-G

43175275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83468399-G-A

http://identifiers.org/hco/22/GRCh38#43175298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83468422-C-A

http://identifiers.org/hco/22/GRCh38#43175321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83468445-C-A

http://identifiers.org/hco/22/GRCh38#43175341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83468464-C-A

43175341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83468464-C-G

http://identifiers.org/hco/22/GRCh38#43175362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83468484-C-A

43175362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83468484-C-T

43176273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83468811-G-T

43176298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83468836-G-A

43176298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83468836-G-T

43176310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83468847-G-A

43176310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83468847-G-C

43176310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83468847-G-T

43176364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83468901-T-A

43176364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83468901-T-C

43178643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83469791-G-C

http://identifiers.org/hco/22/GRCh38#43178890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83469994-A-C

43179318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83470810-G-A

43179339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83470831-C-T

http://identifiers.org/hco/22/GRCh38#43179520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83470955-C-A

43179520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83470955-C-T

http://identifiers.org/hco/22/GRCh38#43179527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83470962-C-A

43179527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83470962-C-T

43179543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83470975-A-G

43179559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83470991-A-G

http://identifiers.org/hco/22/GRCh38#43179578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83471010-C-A

43179578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471010-C-T

43179622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: stop gained
orthologous variants: 83471055-G-T

43179756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83471189-T-C

43179804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471237-A-G

43179950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83471384-C-T

43180030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471464-G-A

43180030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471464-G-T

http://identifiers.org/hco/22/GRCh38#43180035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83471469-C-A

43180035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471469-C-G

43180035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471469-C-T

http://identifiers.org/hco/22/GRCh38#43180043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83471477-C-A

43180043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471477-C-T

43180045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471479-C-T

http://identifiers.org/hco/22/GRCh38#43180048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83471482-C-A

43180048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471482-C-T

43180049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471483-G-A

43180049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471483-G-C

43180049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83471483-G-T

43180928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83472890-G-A

http://identifiers.org/hco/22/GRCh38#43180944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83472906-C-A

43180944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83472906-C-T

http://identifiers.org/hco/22/GRCh38#43181851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83474281-A-C

43181855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83474285-T-C

43182467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475127-G-T

http://identifiers.org/hco/22/GRCh38#43182770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83475425-C-A

43182770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475425-C-T

43182794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475454-C-T

43183006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83475606-G-A

43183063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83475663-C-T

43183141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83475741-G-A

43183141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: missense variant
orthologous variants: 83475741-G-C

43183141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: missense variant
orthologous variants: 83475741-G-T

43183180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475779-G-A

http://identifiers.org/hco/22/GRCh38#43183193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83475792-C-A

43183193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475792-C-G

http://identifiers.org/hco/22/GRCh38#43183194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83475793-C-A

43183194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475793-C-T

43183195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475794-C-T

http://identifiers.org/hco/22/GRCh38#43183199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83475798-C-A

43183199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475798-C-T

43183208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475807-T-A

43183333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83475879-T-C

43184018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83476564-A-T

43184021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83476567-C-G

43184137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83476669-G-A

43184180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83476684-G-T

43185343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83477489-C-T

43185406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83477556-G-A

43185638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83477738-C-T

http://identifiers.org/hco/22/GRCh38#43185720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83477806-A-C

43185736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83477821-C-G

43185795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83477893-G-A

43185950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83478073-G-A

43186352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: 83478668-G-A

43186748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, undefined
orthologous variants: 83479052-C-T

http://identifiers.org/hco/22/GRCh38#43186751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#83479055-C-A

43186751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, undefined
orthologous variants: 83479055-C-T

http://identifiers.org/hco/22/GRCh38#43186777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83479068-C-A

http://identifiers.org/hco/22/GRCh38#43186851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#83479104-C-A

43186851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: intron_variant, undefined
orthologous variants: 83479104-C-T

43186983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83479240-G-A

43186983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83479240-G-C

43186983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83479240-G-T

http://identifiers.org/hco/22/GRCh38#43187013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83479270-C-A

43187013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: missense variant
orthologous variants: 83479270-C-G

43187013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: synonymous variant
orthologous variants: 83479270-C-T

43187088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 5 prime UTR variant
orthologous variants: 83479323-G-A

43187088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 5 prime UTR variant
orthologous variants: 83479323-G-C

43187088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28974
most severe consequence: 5 prime UTR variant
orthologous variants: 83479323-G-T