174072606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72921442-T-C

174072733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72921715-G-T

174073517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72922154-T-C

174073632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72922242-C-T

174074180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72922764-G-A

174074312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72922871-G-T

http://identifiers.org/hco/2/GRCh38#174074313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72922872-C-A

174074313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72922872-C-T

http://identifiers.org/hco/2/GRCh38#174074337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72922894-C-A

174074337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72922894-C-T

174074352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72922912-A-G

174074368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72922936-G-A

174074507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72923058-T-A

174074719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72923256-C-T

http://identifiers.org/hco/2/GRCh38#174074854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72923392-C-A

174074854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3 prime UTR variant
orthologous variants: 72923392-C-T

http://identifiers.org/hco/2/GRCh38#174075385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72923927-C-A

174075385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72923927-C-G

174075385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72923927-C-T

174075438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72923979-C-T

174075549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72924088-G-T

174075564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72924102-T-A

174075564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72924102-T-C

http://identifiers.org/hco/2/GRCh38#174075618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72924243-C-A

174075834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72924465-G-C

174075997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72924622-T-G

174076095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72924834-C-T

174076377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72925143-C-T

http://identifiers.org/hco/2/GRCh38#174076472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72925210-C-A

174076637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72925382-T-C

174077341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72925965-C-T

http://identifiers.org/hco/2/GRCh38#174077445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72926055-C-A

174077940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72926524-T-C

174078198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72926768-A-G

174078523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72927053-T-C

174078912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72927429-C-T

http://identifiers.org/hco/2/GRCh38#174078933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72927450-C-A

174078977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72927498-A-G

http://identifiers.org/hco/2/GRCh38#174079203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72927721-C-A

http://identifiers.org/hco/2/GRCh38#174079224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72927742-A-C

174079240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72927758-A-G

174079267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72927789-T-G

174079327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72927853-T-C

174079342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72927868-G-T

174079356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72927882-G-C

174079356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72927882-G-T

174079357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72927883-T-C

http://identifiers.org/hco/2/GRCh38#174079401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72927926-A-C

174079484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72928012-T-A

174079728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72928242-C-T

174080453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72928948-G-A

174080527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72929023-T-C

http://identifiers.org/hco/2/GRCh38#174080772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72929256-C-A

174080904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72929388-T-C

http://identifiers.org/hco/2/GRCh38#174081061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72929545-C-A

174081061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72929545-C-T

174081125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72929609-T-C

174081272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72929756-A-T

174081624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72930118-T-G

174082515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72931001-G-A

174082686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72931189-A-G

174082955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72931430-T-C

http://identifiers.org/hco/2/GRCh38#174083133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72931621-A-C

174083214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72931839-G-A

174083395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72932207-C-T

174083399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72932211-A-G

174084469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72933439-A-G

174084730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72933694-G-A

174084926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72933864-G-C

174085758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72934314-T-C

174086170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72936124-T-C

174086270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72936207-G-A

174087836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937233-C-T

174087984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937450-A-G

174087995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937541-T-C

174088129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937656-G-T

174088206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937693-C-T

174088207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937694-A-G

174088223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937709-G-A

174088329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937806-G-A

http://identifiers.org/hco/2/GRCh38#174088439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72937964-C-A

174088439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937964-C-G

174088439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937964-C-T

174088457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72937984-C-T

http://identifiers.org/hco/2/GRCh38#174088541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72938092-C-A

http://identifiers.org/hco/2/GRCh38#174088731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72938157-C-A

174088927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72938287-C-T

174089377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72938695-A-G

174090196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72939156-G-A

174090797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72940032-C-T

174090801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72940036-C-T

174091390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

174091577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

174093718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72944232-A-G

174096046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72944573-T-C

174096074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72944604-G-C

http://identifiers.org/hco/2/GRCh38#174096700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72945311-C-A

174096700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72945311-C-G

174096755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72945351-C-T

174097340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72945576-C-T

174098250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72945968-T-C

174098307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72946030-T-C

174098440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72946159-C-G

174098595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72946638-C-T

174098640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72946685-G-A

174098877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72946902-G-A

174098961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72946985-C-T

174099121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72949240-G-A

174099739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72949811-T-C

174100194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72950277-T-C

174103087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72952121-C-G

174103087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72952121-C-T

174103268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72952279-T-C

174103713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72953387-C-T

http://identifiers.org/hco/2/GRCh38#174104258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72953848-C-A

174104352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72953938-C-T

174104559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72954152-C-G

http://identifiers.org/hco/2/GRCh38#174104610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72954183-C-A

http://identifiers.org/hco/2/GRCh38#174104778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72954338-C-A

174104801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72954361-T-A

174105332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72954894-T-C

174105342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72954904-C-T

174105979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72955526-A-G

http://identifiers.org/hco/2/GRCh38#174106050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72955593-A-C

174106412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72955962-C-T

174107145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72956680-C-T

http://identifiers.org/hco/2/GRCh38#174107318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72956852-C-A

174109162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72958649-T-C

174109191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72958674-C-T

174109194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72958677-T-C

174109450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72958930-C-T

174111190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72959781-C-T

174111307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72959895-C-G

174111522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72960104-T-A

http://identifiers.org/hco/2/GRCh38#174111569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72960157-C-A

174111569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72960157-C-T

174111940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72961204-A-G

174112095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72961522-A-T

174116323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72964844-T-C

174116438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72964949-A-G

174116438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72964949-A-T

174116571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72965062-G-A

174116677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72965165-T-C

174117040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72965584-T-C

174117444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72966108-A-G

174117716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72966741-T-C

174117757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72966771-C-G

174119420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72968459-T-C

174119496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72968532-T-C

174119496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72968532-T-G

174120496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72969405-T-A

174120515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72969424-C-T

174122059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72971091-C-T

174122664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72971688-T-C

174123326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72972388-T-A

174123326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72972388-T-C

http://identifiers.org/hco/2/GRCh38#174123477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72972538-C-A

http://identifiers.org/hco/2/GRCh38#174123547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72972608-C-A

174123735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72972791-T-C

174123737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72972793-T-A

http://identifiers.org/hco/2/GRCh38#174124401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72973373-C-A

174125465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72974447-C-T

174125853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72974781-T-C

174125858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72974786-T-C

174126001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72974809-T-C

174126071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72974878-T-C

174126187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72974987-C-G

174134786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72983733-T-A

174134937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72983915-G-A

174134975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72983947-C-T

174141809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987066-G-A

174141831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: synonymous variant
orthologous variants: 72987088-A-G

174141972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 72987229-G-A

174142045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987307-G-T

http://identifiers.org/hco/2/GRCh38#174142046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72987308-C-A

174142046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987308-C-T

174142076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987338-T-A

174142076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987338-T-C

174142104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987360-T-C

174142123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987376-G-A

174142123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987376-G-C

174142123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987376-G-T

174142132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987385-G-T

174142286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72987523-T-C

174142983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72988195-T-A

174143060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72988272-C-T

174143087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72988299-A-G

174143144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72988356-G-A

174151064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72990291-G-A

174151588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72991910-T-C

174151764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72992238-T-C

174151869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72992337-C-T

174151937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72992401-C-T

174152088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72992529-G-A

174152389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72992812-T-C

174153091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72993853-T-C

174154264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72994687-C-T

174155309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72995500-C-T

174155325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72995484-T-C

174155352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72995453-G-A

174157576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72997109-G-A

174157788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72997293-G-A

174157788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72997293-G-T

174157923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72997413-T-C

http://identifiers.org/hco/2/GRCh38#174158172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#72997639-A-C

174158377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72997846-G-T

174158503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72997948-G-A

174158503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72997948-G-C

174158582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72998030-T-A

174158658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72998117-G-A

174158658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72998117-G-C

174159596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72998995-G-A

174160380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 72999739-C-T

174160654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73000002-C-T

174161092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73000438-G-A

174161952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73000959-A-T

174162058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73001068-T-C

174162124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73001137-G-A

174162306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73001302-C-T

174164508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73002953-C-T

174164615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73003068-A-T

174164859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73003426-G-A

174175949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73009520-A-G

174176025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73009563-G-A

174176388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73009862-A-G

174176834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73010252-C-T

174177474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73010887-A-G

174178308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73012360-A-T

174179709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73013686-G-A

174179717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73013692-T-C

http://identifiers.org/hco/2/GRCh38#174179741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73013716-C-A

174179826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73013780-A-T

174179997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73013949-A-T

174193744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73017046-A-G

174194285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73017467-A-G

174195734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73019304-G-A

174195839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73019587-T-A

174195989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73019743-A-G

174196095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73019846-A-T

174196555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73020288-T-G

174206656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73022770-G-A

174207144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73023265-T-A

174207271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73023382-C-G

174207338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73023453-C-G

http://identifiers.org/hco/2/GRCh38#174222970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73029702-C-A

174222970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73029702-C-T

174223216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73029918-C-G

174223231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73029933-A-G

174223236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73029938-T-C

174223254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73029960-C-T

http://identifiers.org/hco/2/GRCh38#174223300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73030011-C-A

174223300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73030011-C-G

174223300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73030011-C-T

174223370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73031364-G-T

174229499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73033865-G-A

174229499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73033865-G-T

174229509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73033876-T-C

174232135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73037910-G-A

174232450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73038318-A-G

174243445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73039713-C-T

174243681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73039903-G-C

174243901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73040828-G-A

174245096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73041852-G-A

174245246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73041997-C-G

174245246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73041997-C-T

174245341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73042085-C-T

174245411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73042155-A-T

174245755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73042503-G-A

174245791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73042538-G-A

174246934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73043406-T-C

174246986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73043459-G-T

174247403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73043528-G-A

174247403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73043528-G-T

http://identifiers.org/hco/2/GRCh38#174247521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73043637-C-A

http://identifiers.org/hco/2/GRCh38#174247667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73043768-C-A

174247667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron variant
orthologous variants: 73043768-C-T

174247719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, missense_variant
orthologous variants: 73043821-G-A

http://identifiers.org/hco/2/GRCh38#174247828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73044018-C-A

http://identifiers.org/hco/2/GRCh38#174247838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73044025-C-A

174247838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044025-C-T

http://identifiers.org/hco/2/GRCh38#174247919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#73044110-A-C

http://identifiers.org/hco/2/GRCh38#174248059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73044268-C-A

174248059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044268-C-T

174248124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044321-C-T

174248138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044335-G-A

174248161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044372-G-A

174248161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044372-G-T

http://identifiers.org/hco/2/GRCh38#174248163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73044374-C-A

174248163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044374-C-G

http://identifiers.org/hco/2/GRCh38#174248212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73044423-C-A

174248212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044423-C-G

174248212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044423-C-T

174248228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044438-G-A

174248228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73044438-G-T

http://identifiers.org/hco/2/GRCh38#174248331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#73044532-A-C

174248433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, undefined
orthologous variants: 73044611-G-A

174248433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, undefined
orthologous variants: 73044611-G-C

174248433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: intron_variant, undefined
orthologous variants: 73044611-G-T

174248518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 73044693-G-C

174248518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 73044693-G-T

http://identifiers.org/hco/2/GRCh38#174248599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#73044770-C-A

174248599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28833
most severe consequence: 5 prime UTR variant
orthologous variants: 73044770-C-T