174432270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73171882-T-G

174432511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73172116-C-T

http://identifiers.org/hco/2/GRCh38#174432582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73172162-C-A

http://identifiers.org/hco/2/GRCh38#174432624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73172208-A-C

174432624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73172208-A-G

174432768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73172321-T-A

174432768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73172321-T-G

174433105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73172348-A-G

http://identifiers.org/hco/2/GRCh38#174433109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73172352-C-A

174433109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73172352-C-T

174433801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73172731-G-T

174434291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73172898-A-T

174434335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73172928-T-A

174434494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73173059-G-T

174434955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73173357-G-T

http://identifiers.org/hco/2/GRCh38#174434957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73173359-C-A

174434965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73173367-T-A

174435054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73173448-G-T

174435896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73173621-G-T

174435968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73173687-G-A

174435968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73173687-G-T

174436039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73173727-G-T

174436083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 3 prime UTR variant
orthologous variants: 73173772-T-A

174436154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: missense variant
orthologous variants: 73173839-C-T

174436196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: missense variant
orthologous variants: 73173881-T-C

174436314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73173999-G-A

174436314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 73173999-G-T

174436470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73174157-G-T

174436949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73176418-C-G

174438267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73177187-G-C

http://identifiers.org/hco/2/GRCh38#174439178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73177944-C-A

174439628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178354-G-A

174439821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178418-G-A

174439821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178418-G-T

174439978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73178561-T-C

174440039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73178622-A-G

174440128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178653-A-G

174440146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178670-G-C

174440159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178683-A-G

http://identifiers.org/hco/2/GRCh38#174440164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73178685-C-A

174440164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178685-C-G

174440185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178709-G-A

174440185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178709-G-T

174440199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178723-C-T

174440494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178883-A-G

http://identifiers.org/hco/2/GRCh38#174440501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73178890-A-C

174440501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73178890-A-G

174440760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73179211-C-T

http://identifiers.org/hco/2/GRCh38#174440850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73179479-C-A

174441002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73179694-C-T

174441117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73179806-A-G

174441117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73179806-A-T

174442178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73180030-A-G

174442325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73180168-G-A

174442836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73180723-C-T

http://identifiers.org/hco/2/GRCh38#174442877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#73180763-C-A

174442891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73180777-G-T

174442905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73180791-G-A

174442946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73180824-G-C

174443309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181213-G-A

174443378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181287-T-C

174443728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181466-A-T

174443878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73181583-G-A

174445059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73182173-A-T

174445152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73182264-G-T

174445162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73182274-A-G

174445180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73182292-T-A

174445180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73182292-T-C

174445181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 73182293-A-G

174445280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73182386-A-G

174445283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73182389-A-G

174445375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73182481-A-G

174445398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73182503-G-A

174445398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73182503-G-T

http://identifiers.org/hco/2/GRCh38#174445427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73182532-A-C

174445439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73182544-T-C

174445439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73182544-T-G

174445443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73182548-T-A

174445473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73182577-T-A

174445498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73182602-T-G

http://identifiers.org/hco/2/GRCh38#174445525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73182632-C-A

http://identifiers.org/hco/2/GRCh38#174445603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73182709-A-C

174445628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73182737-T-C

174445657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73182765-A-G

174446457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73183814-C-T

174446578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73183925-T-C

http://identifiers.org/hco/2/GRCh38#174446585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73183932-A-C

174446629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: 73183979-G-A

174446629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: 73183979-G-T

174446850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73184155-A-G

174446995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73184273-A-G

174447014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73184286-A-G

174447016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73184288-A-G

174453699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73186904-G-A

174453699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73186904-G-T

174453779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: missense variant
orthologous variants: 73186984-T-C

174453800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: missense variant
orthologous variants: 73187005-G-A

174453861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73187066-T-C

http://identifiers.org/hco/2/GRCh38#174453876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73187081-C-A

174453876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73187081-C-T

174453891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73187096-T-C

174455445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73188910-T-A

174455770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73189179-T-G

http://identifiers.org/hco/2/GRCh38#174459391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73192317-A-C

174459399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73192325-T-C

http://identifiers.org/hco/2/GRCh38#174459589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73192407-A-C

http://identifiers.org/hco/2/GRCh38#174459695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73192502-A-C

174459819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73192669-G-A

174459819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73192669-G-T

174459826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73192678-T-C

174459835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73192687-A-T

174459897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: 73192788-T-G

174459913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: missense variant
orthologous variants: 73192804-T-A

174460131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73193022-T-A

174460131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73193022-T-C

174460131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73193022-T-G

174460414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73193440-G-A

174460414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73193440-G-T

174460724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73193713-C-T

174461202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194105-G-T

174461284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194171-G-T

174461366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194241-T-C

174461366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194241-T-G

174461369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194244-T-G

174461382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194256-T-C

174461387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194261-G-T

http://identifiers.org/hco/2/GRCh38#174461477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73194351-A-C

174461495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73194369-G-A

174461495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73194369-G-T

174461516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194384-A-G

174461517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194385-G-A

174461517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194385-G-T

http://identifiers.org/hco/2/GRCh38#174461521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73194389-A-C

174461557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194465-G-T

http://identifiers.org/hco/2/GRCh38#174461579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73194504-C-A

174461579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194504-C-T

174461712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73194641-A-G

174462800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73195235-T-G

http://identifiers.org/hco/2/GRCh38#174462830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73195309-A-C

174463061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73195514-C-T

http://identifiers.org/hco/2/GRCh38#174463577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73195711-A-C

174463669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73195845-G-A

174463897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73195982-T-C

174464122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73196063-A-G

174464301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73196203-T-C

174464764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73196702-C-T

174465241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197355-T-A

174465394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197506-G-A

174465480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, undefined
orthologous variants: 73197579-C-T

174465633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197671-T-C

174465645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197683-C-T

174465653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197691-G-A

http://identifiers.org/hco/2/GRCh38#174465661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73197699-C-A

174465663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197701-G-A

174465663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197701-G-C

174465663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197701-G-T

174465669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197707-G-C

174465717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197763-G-A

174465717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197763-G-C

174465717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197763-G-T

174465734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197780-A-G

174465734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197780-A-T

174465915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73197956-T-A

http://identifiers.org/hco/2/GRCh38#174465947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73197990-C-A

174465993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73198034-T-C

174466036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73198075-T-A

174466036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73198075-T-C

174466036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73198075-T-G

174466488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73198603-A-G

http://identifiers.org/hco/2/GRCh38#174466489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73198604-C-A

174466489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73198604-C-G

174466489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73198604-C-T

174468058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73199513-T-C

174468138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73199596-A-G

174468139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73199597-T-C

174468327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73199758-C-T

174468656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200061-C-T

174468783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200188-A-G

174468783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200188-A-T

174468897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200315-A-G

174468897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200315-A-T

174468954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: missense variant
orthologous variants: 73200372-C-G

174469062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: 73200480-G-A

174469177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200596-A-G

174469185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200604-T-C

http://identifiers.org/hco/2/GRCh38#174469206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73200625-C-A

174469206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200625-C-T

http://identifiers.org/hco/2/GRCh38#174469216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73200635-C-A

174469216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200635-C-G

http://identifiers.org/hco/2/GRCh38#174469314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73200717-A-C

174469402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200805-G-A

174469477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200878-T-C

174469657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73200979-T-C

174469846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201189-T-G

174470328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201238-T-A

174470328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201238-T-C

174470328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201238-T-G

174470343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201255-T-C

174470465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: 73201384-T-C

http://identifiers.org/hco/2/GRCh38#174470676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73201604-C-A

174470676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201604-C-T

174470727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201645-A-T

174470733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201651-A-T

174471441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201982-G-A

174471441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73201982-G-T

174471537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73202070-T-C

174471830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73202868-T-A

174472109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73203079-T-C

174472917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73203907-T-C

174472956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73203950-G-A

174472956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73203950-G-T

174473186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: 73204180-A-G

174473257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: missense variant
orthologous variants: 73204251-T-C

http://identifiers.org/hco/2/GRCh38#174473480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73204469-C-A

174473795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73204788-A-T

174473830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73204815-T-C

http://identifiers.org/hco/2/GRCh38#174473834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73204866-A-C

174473897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73204973-G-T

174474059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205122-C-T

174474070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205130-C-T

174474093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205154-T-C

174474093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205154-T-G

174474157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205213-G-A

174474166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205222-A-G

174474182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205238-G-C

174474182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205238-G-T

174474447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205461-C-T

174474514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205527-C-T

174474744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205685-G-C

174474747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73205688-G-A

http://identifiers.org/hco/2/GRCh38#174474859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73205800-C-A

174475671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73206277-C-T

174475751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73206349-C-T

174476238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73207117-C-T

174476721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73207309-T-C

174476844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73207434-G-A

174476844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73207434-G-C

174476844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73207434-G-T

174477085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73207650-T-G

174479118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73209724-G-A

174479707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73210692-T-G

174479730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73210715-G-A

174479730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73210715-G-T

174479963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73210919-T-C

174480164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73211091-G-C

174480458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73211367-T-C

http://identifiers.org/hco/2/GRCh38#174480480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73211389-A-C

174480659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73211542-T-G

174480738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73211609-C-T

174481395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73211994-G-T

174481621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: 73212292-A-G

174481843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: 73212514-T-A

174481858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: missense variant
orthologous variants: 73212529-G-T

174481936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: synonymous variant
orthologous variants: 73212601-T-C

http://identifiers.org/hco/2/GRCh38#174482085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73212749-C-A

174482085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73212749-C-T

http://identifiers.org/hco/2/GRCh38#174482102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73212766-C-A

174482102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73212766-C-T

174482121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron variant
orthologous variants: 73212770-A-T

174483098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73213667-C-T

174483106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73213675-G-A

174483107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73213676-G-A

174483107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73213676-G-T

174483302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73213874-A-G

174484071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73214261-G-A

174484071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73214261-G-C

174484071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73214261-G-T

174484095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73214285-C-T

174484125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73214314-A-G

174484264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73214451-A-G

174484461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73214660-T-G

174484495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73214730-A-G

174484817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73215000-G-A

174484992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73215108-A-G

174485037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73215151-G-T

174485164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73215312-G-C

174485164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73215312-G-T

174486140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 73216083-C-T

174486612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73216395-A-G

174486922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 73216656-G-A

174486922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 73216656-G-T

http://identifiers.org/hco/2/GRCh38#174486989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73216717-C-A

174486989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 73216717-C-T

http://identifiers.org/hco/2/GRCh38#174487068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73216807-C-A

174487068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5 prime UTR variant
orthologous variants: 73216807-C-T

http://identifiers.org/hco/2/GRCh38#174487093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#73216826-C-A

174487093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22951
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 73216826-C-T