118813714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53412385-T-A

http://identifiers.org/hco/6/GRCh38#118814182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53412757-C-A

118814196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53412771-T-C

118814233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53412798-A-G

118814359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53412921-C-T

118814516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413081-T-C

118814564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413149-A-G

118814597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413212-T-C

118814630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413245-G-A

118814630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413245-G-C

http://identifiers.org/hco/6/GRCh38#118814633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53413248-C-A

118814633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413248-C-T

118814645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413260-T-C

118814664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413278-A-G

118814728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413329-C-T

118814753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413350-A-G

118814802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53413398-T-C

http://identifiers.org/hco/6/GRCh38#118814848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53413444-A-C

http://identifiers.org/hco/6/GRCh38#118814917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53413513-C-A

118814917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53413513-C-T

118814950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53413546-T-A

118814950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53413546-T-C

118815024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53413644-T-C

118815033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53413653-G-A

118815033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53413653-G-T

118815160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53413780-A-G

118815169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53413789-A-G

118815251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53413871-C-T

118815259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53413879-C-T

118815260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53413880-T-C

118815463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53414083-C-G

118815594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53414202-G-A

118815602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414210-T-C

http://identifiers.org/hco/6/GRCh38#118815655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53414263-A-C

118815671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414279-T-C

118815714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53414322-G-A

118815750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414343-G-A

118815750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414343-G-T

118815808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414398-T-G

118815812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414402-A-G

http://identifiers.org/hco/6/GRCh38#118815836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53414426-C-A

118815836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414426-C-T

118816035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414625-T-A

118816035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414625-T-G

118816046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414636-T-A

118816046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53414636-T-G

http://identifiers.org/hco/6/GRCh38#118816099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53414689-A-C

118816105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53414695-T-C

118816105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53414695-T-G

http://identifiers.org/hco/6/GRCh38#118816301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53414869-C-A

118816373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53414931-G-A

118816373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53414931-G-T

118816377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53414935-T-C

118816380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53414938-C-T

118816389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53414947-G-T

118816464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415001-T-A

118816853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415346-T-C

118816876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415362-T-A

118816876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415362-T-C

118816986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415468-T-C

118823637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415612-G-T

118823727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415696-G-C

118824162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415978-A-G

118824733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53416330-A-G

118824764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53416361-T-A

118824764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53416361-T-C

118825125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53416689-C-T

118825314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53416820-A-G

118825377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53416859-A-T

118826139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53417026-T-A

118826139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53417026-T-C

118826143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417030-T-C

http://identifiers.org/hco/6/GRCh38#118826173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53417060-C-A

118826173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53417060-C-G

118826173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53417060-C-T

118826387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417271-G-A

118826387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417271-G-T

118826438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417318-A-G

118826457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417337-C-T

118826523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417409-T-C

118826556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417442-C-T

118826633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417515-A-G

118826633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417515-A-T

118826688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417558-T-G

118826700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417570-T-G

118826726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417596-T-A

118826726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417596-T-C

118826753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417615-T-C

118826773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417624-T-C

http://identifiers.org/hco/6/GRCh38#118826794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53417645-C-A

118826794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53417645-C-G

118826794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53417645-C-T

118826806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53417657-C-T

http://identifiers.org/hco/6/GRCh38#118826810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53417661-A-C

118826810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53417661-A-G

118826817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53417668-T-C

118826860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53417711-A-G

118826892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417736-T-C

118826894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417738-G-C

118826894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417738-G-T

118826906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417750-G-T

118826917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417761-A-G

118826946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417790-T-C

118826946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417790-T-G

118826955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417799-T-C

http://identifiers.org/hco/6/GRCh38#118827012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53417837-C-A

118827012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417837-C-G

118827012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417837-C-T

118827059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417883-A-G

118827098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53417920-T-C

118827202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53418022-T-C

118827501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53418320-T-C

118827540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53418355-C-T

http://identifiers.org/hco/6/GRCh38#118827545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53418360-A-C

118827644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423027-T-C

118827778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423355-C-T

http://identifiers.org/hco/6/GRCh38#118827834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53423415-A-C

118827860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423440-T-C

118827889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423461-G-A

118827889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423461-G-T

http://identifiers.org/hco/6/GRCh38#118827890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53423462-C-A

118827892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423464-T-C

118828107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53423679-G-A

118828144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423716-G-A

http://identifiers.org/hco/6/GRCh38#118828173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53423746-C-A

118828428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423974-C-G

http://identifiers.org/hco/6/GRCh38#118828683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53424203-C-A

118828683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424203-C-T

118828724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424241-T-G

118828767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424291-G-A

118828827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424391-T-C

118828828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424392-A-G

118828838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424400-G-A

118828854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424416-G-A

http://identifiers.org/hco/6/GRCh38#118828904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53424463-C-A

118828947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424500-T-C

118829032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53424577-G-C

118829169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53424714-C-T

118829184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53424729-G-T

118829187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53424732-G-A

118829304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424847-G-T

118829357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424902-C-G

118829357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424902-C-T

118829599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425157-T-C

118830175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53428061-T-A

118830509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53428390-A-G

http://identifiers.org/hco/6/GRCh38#118843195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53431064-C-A

http://identifiers.org/hco/6/GRCh38#118843830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53431311-C-A

118844130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53431628-T-C

118844912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433620-G-A

118845115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433822-T-C

118845115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433822-T-G

118845127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53433836-C-T

http://identifiers.org/hco/6/GRCh38#118845282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53433918-A-C

118845947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434882-A-G

118850344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53435295-T-A

118850643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53436162-A-G

118850703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53436242-T-C

118850779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53436321-C-T

118851777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53437167-A-G

118851800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53437187-A-G

118856082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53438833-A-G

118856254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53439276-T-C

118856255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53439277-A-G

http://identifiers.org/hco/6/GRCh38#118856339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53439342-A-C

http://identifiers.org/hco/6/GRCh38#118856346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53439349-C-A

118856346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53439349-C-T

118856352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53439355-A-G

118856581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53439589-T-C

118888559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467342-A-G

118888580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467363-C-T

118888637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467413-T-C

118888685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467459-C-T

118888715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467488-T-A

118888715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467488-T-C

118888847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467679-C-T

118888890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467759-A-G

118888926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467791-T-C

118888930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467795-G-A

118888944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467811-G-A

118889095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467950-G-A

118889109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467965-A-T

118889129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467985-C-T

118889222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468022-C-T

http://identifiers.org/hco/6/GRCh38#118889320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53468101-C-A

118889344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468125-G-A

118889464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468244-C-T

118889485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468266-C-T

http://identifiers.org/hco/6/GRCh38#118889802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53468536-C-A

118889875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468608-C-T

118889893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468626-G-A

118889895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468628-A-G

118889943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468678-G-A

118890026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468991-C-T

118890033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468998-C-T

118890429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53469365-A-G

118890986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470205-T-C

118891062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53470270-G-A

118891062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53470270-G-C

118891842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470854-C-T

118891952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470919-C-G

118892051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470994-T-G

118892312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471241-T-G

118892652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53471510-A-T

http://identifiers.org/hco/6/GRCh38#118893162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53471962-C-A

118893162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53471962-C-T

118893497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53472343-G-A

118893497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53472343-G-C

http://identifiers.org/hco/6/GRCh38#118893581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#53472425-A-C

http://identifiers.org/hco/6/GRCh38#118893660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#53472486-C-A

118893791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53472628-G-A

118893791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53472628-G-C

http://identifiers.org/hco/6/GRCh38#118893849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53472670-A-C

118893908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53472754-G-A

118893908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53472754-G-C

118893908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53472754-G-T

http://identifiers.org/hco/6/GRCh38#118893941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#53472814-C-A

118893941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53472814-C-T

http://identifiers.org/hco/6/GRCh38#118893943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#53472816-C-A

http://identifiers.org/hco/6/GRCh38#118893957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#53472835-C-A

118893957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53472835-C-T

http://identifiers.org/hco/6/GRCh38#118893984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53472858-C-A

118893984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53472858-C-G

118894329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53473206-T-A

118894329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53473206-T-C

118894329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53473206-T-G

118894367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53473243-G-T

118896048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53474566-T-G

118896338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53474841-C-T

118896440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53474934-T-C

118896446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53474940-A-G

118896789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53475253-A-G

118897383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53475490-G-A

118897575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53475640-C-G

118897691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53475724-G-T

http://identifiers.org/hco/6/GRCh38#118897841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53475856-C-A

118899093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53476553-G-A

118899093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53476553-G-C

118899207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53476673-A-G

118899347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53477070-C-T

118899466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53477185-G-A

118899723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53477428-T-C

http://identifiers.org/hco/6/GRCh38#118899929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53477578-C-A

118899981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53477643-G-T

118900131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53477786-G-A

118900131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53477786-G-C

118900181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53477832-G-A

118900193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53477844-A-G

118900203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53477854-G-A

118900204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53477855-T-C

118900414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478131-T-C

http://identifiers.org/hco/6/GRCh38#118900625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53478325-C-A

118900625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478325-C-G

118900697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478378-A-G

118900698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478379-G-A

118900698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478379-G-C

http://identifiers.org/hco/6/GRCh38#118900714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53478392-C-A

118900714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478392-C-T

118900782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53478460-T-G

118900854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53478532-C-T

http://identifiers.org/hco/6/GRCh38#118900996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53478658-C-A

http://identifiers.org/hco/6/GRCh38#118901010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53478672-C-A

118901010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53478672-C-G

118901034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53478691-T-C

118901049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478704-G-T

118901050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478705-G-A

118901050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478705-G-T

118901182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478804-A-G

118901746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479265-T-G

118902097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479576-A-G

118902252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479691-C-T

118902278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479702-C-T

118902470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479868-C-T

118902471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479869-T-G

118902841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480167-A-G

http://identifiers.org/hco/6/GRCh38#118903284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53480500-C-A

118903284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480500-C-T

118903378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480581-C-T

118903604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480706-A-G

118903642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480741-C-T

118904104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480921-C-T

http://identifiers.org/hco/6/GRCh38#118904116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53480933-A-C

118904116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480933-A-G

118904151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480967-G-A

118904304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53481103-A-G

http://identifiers.org/hco/6/GRCh38#118904399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53481195-C-A

118904399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53481195-C-T

118904632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53481387-T-C

118904648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53481401-T-G

118905358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53481824-G-C

118905565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482125-T-G

118905581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482142-A-G

118905777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53482330-T-C

118905834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482387-G-A

118905834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482387-G-C

118905870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482423-A-G

118905916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482461-A-T

118905971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482510-A-G

118906715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483012-C-T

118907007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483291-A-T

118907125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483496-A-G

http://identifiers.org/hco/6/GRCh38#118907215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53483598-C-A

118907228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483608-C-T

118907233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483613-C-T

118907234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483614-G-A

http://identifiers.org/hco/6/GRCh38#118907268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53483644-C-A

118907268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483644-C-T

118907976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53484318-G-T

118908260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53484565-T-C

118908295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53484602-G-T

118908438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53484721-G-A

118908547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53484779-G-T

118908941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53485167-C-T

118909031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53485257-C-T

118909174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53485367-G-T

118909385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53485556-C-T

118909499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53485700-C-T

118909526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53485807-T-C

118909526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53485807-T-G

http://identifiers.org/hco/6/GRCh38#118909593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53485905-A-C

118909693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486012-C-T

http://identifiers.org/hco/6/GRCh38#118909698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53486017-A-C

118910397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486452-C-T

118910499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486551-A-G

118910539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486579-A-G

118910541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486581-G-A

118910541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486581-G-T

118910542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486582-G-C

118910542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486582-G-T

http://identifiers.org/hco/6/GRCh38#118910543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53486583-C-A

118910543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486583-C-T

118910559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486599-G-T

118910878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53486813-T-C

http://identifiers.org/hco/6/GRCh38#118911120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53487000-C-A

118911221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53487092-C-G

118911432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53487249-A-G

http://identifiers.org/hco/6/GRCh38#118911480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53487275-A-C

118911480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53487275-A-G

http://identifiers.org/hco/6/GRCh38#118911524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53487316-A-C

118911524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53487316-A-G

118911573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53487375-T-A

118911573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53487375-T-C

http://identifiers.org/hco/6/GRCh38#118911627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53487427-C-A

118911627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53487427-C-T

118911704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53487502-C-T

118911733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53487531-G-A

118911733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53487531-G-C

http://identifiers.org/hco/6/GRCh38#118912192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53487887-C-A

118912517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488201-A-G

118912926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488546-G-A

118912926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488546-G-T

118913108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488668-G-A

118913108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488668-G-T

118913130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488690-G-A

118913130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488690-G-T

118913140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488702-T-A

118913140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488702-T-C

118913236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488863-A-G

118913263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53488891-A-G

118913305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53488933-T-G

118913373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53489001-A-G

118913467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489090-C-T

118913675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489254-T-C

118913984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489527-A-G

118914028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489562-G-A

118914725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490222-G-A

118915638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490641-G-A

118915681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490676-A-G

118915816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490801-C-T

http://identifiers.org/hco/6/GRCh38#118916214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53490992-C-A

118916214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490992-C-G

118916214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490992-C-T

http://identifiers.org/hco/6/GRCh38#118916389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53491151-A-C

118916389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491151-A-G

118917194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53491533-T-C

118917467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53491862-T-C

118917467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53491862-T-G

118917585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53491972-A-G

http://identifiers.org/hco/6/GRCh38#118917643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53492030-C-A

118917815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492201-G-C

118917815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492201-G-T

118917818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492204-T-A

118917818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492204-T-C

118917862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 53492255-A-G

118917994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492387-T-C

118918020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492413-C-G

118918020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492413-C-T

118918068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492453-C-G

http://identifiers.org/hco/6/GRCh38#118918069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53492454-A-C

118918069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492454-A-G

http://identifiers.org/hco/6/GRCh38#118918071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53492456-C-A

118918071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492456-C-T

118918072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492457-A-T

118918082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492467-T-G

http://identifiers.org/hco/6/GRCh38#118918101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53492486-C-A

118918105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492490-G-T

118918313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492624-G-A

118918313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53492624-G-T

118918464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53494169-T-A

118918464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53494169-T-C

118918551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53494257-G-T

118919058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53494493-C-G

118919118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53494554-A-G

118919118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53494554-A-T

118919416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53494776-T-C

http://identifiers.org/hco/6/GRCh38#118919749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53495307-C-A

http://identifiers.org/hco/6/GRCh38#118919794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53495348-C-A

http://identifiers.org/hco/6/GRCh38#118919809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53495363-C-A

118919856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53495402-T-C

118919940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53495434-G-A

118919965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53495456-T-C

http://identifiers.org/hco/6/GRCh38#118921580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53495690-A-C

118921591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53495700-A-G

118921702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53495800-T-C

118921812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53495913-G-A

118921815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53495916-G-T

118921983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53496189-A-G

118922150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53496371-A-G

118922159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53496380-T-C

http://identifiers.org/hco/6/GRCh38#118922191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53496408-A-C

118922191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53496408-A-G

118923658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498700-C-G

118923661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498703-A-G

118923661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498703-A-T

118923664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498706-T-A

118923665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498707-A-G

118923665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498707-A-T

118923725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498765-A-G

118923901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53498942-G-A

118924031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53499072-C-T

118924200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499228-T-C

118924200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499228-T-G

http://identifiers.org/hco/6/GRCh38#118924223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53499253-A-C

118924238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499265-A-G

http://identifiers.org/hco/6/GRCh38#118924241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53499268-A-C

http://identifiers.org/hco/6/GRCh38#118924254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53499312-C-A

118924254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499312-C-T

118924386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499558-G-C

118924386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499558-G-T

118924682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499864-C-T

118924703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53499885-A-T

118930965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501193-T-C

118931063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501274-T-C

118931065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501276-G-T

118931268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501462-T-C

118931289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501487-G-A

118931289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501487-G-T

118931320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501520-A-T

118931404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501796-T-G

118931487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53501879-T-C

118931487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53501879-T-G

118931496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53501888-T-C

http://identifiers.org/hco/6/GRCh38#118931559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53501951-C-A

http://identifiers.org/hco/6/GRCh38#118931718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53502110-A-C

118931718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53502110-A-G

118931736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 53502128-T-A

118931736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 53502128-T-G

118931755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502146-G-A

118931755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502146-G-T

118931764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502155-T-A

118931833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502227-G-T

http://identifiers.org/hco/6/GRCh38#118931850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53502244-C-A

http://identifiers.org/hco/6/GRCh38#118931871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53502261-A-C

118931871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502261-A-G

118931873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502263-C-T

118931893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502283-C-T

http://identifiers.org/hco/6/GRCh38#118932606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53503775-C-A

http://identifiers.org/hco/6/GRCh38#118932656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53503816-C-A

118932714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53503871-G-C

118932744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53503901-T-A

http://identifiers.org/hco/6/GRCh38#118932793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53503944-A-C

http://identifiers.org/hco/6/GRCh38#118932866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53504011-C-A

118932880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53504029-G-A

118932974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53504109-C-T

118933043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53504181-A-G

118933109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53504244-A-G

http://identifiers.org/hco/6/GRCh38#118933990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53505046-C-A

118933990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505046-C-T

118934103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505166-C-G

118934126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505189-A-G

http://identifiers.org/hco/6/GRCh38#118934331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53505399-A-C

118934420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53505485-A-G

118934480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505530-G-A

118934517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53505552-C-T

118934528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53505563-G-A

118934528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53505563-G-T

118934830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53505754-G-A

http://identifiers.org/hco/6/GRCh38#118934956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53505879-C-A

118934975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 53505889-C-T

http://identifiers.org/hco/6/GRCh38#118935096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#53505996-C-A

118935096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53505996-C-G

118935096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53505996-C-T

118935117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53506017-C-T

http://identifiers.org/hco/6/GRCh38#118935121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#53506021-C-A

http://identifiers.org/hco/6/GRCh38#118935162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#53506063-A-C

118935162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53506063-A-G

118935162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53506063-A-T