145936628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42185574-G-A

145936628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42185574-G-T

145936630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42185576-G-A

145936658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42185601-G-T

145936737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42185670-A-G

145936766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42185693-G-A

145936766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42185693-G-T

145936821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42185774-G-A

145936821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42185774-G-T

145937337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42186306-A-T

145937375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42186343-C-T

145937525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42186506-C-T

145937735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42186698-G-A

http://identifiers.org/hco/5/GRCh38#145937746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#42186709-C-A

145937746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42186709-C-T

145937851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42186806-A-G

145937990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 42186944-T-A

145937990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 42186944-T-C

145938054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42187008-G-A

http://identifiers.org/hco/5/GRCh38#145938135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42187089-C-A

145938135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42187089-C-G

145938135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42187089-C-T

145938253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42187207-C-T

145938264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42187218-T-C

145938342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187297-A-G

145938342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187297-A-T

145938376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187332-G-A

145938376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187332-G-T

145938394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187350-A-G

145938413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187383-T-A

145938413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187383-T-C

145938572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187538-C-G

145938902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187859-C-T

145938967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187921-G-A

145939025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187965-G-T

145939039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42187979-A-G

145939221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42188126-T-C

145939455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42188342-T-G

145939569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42188458-A-T

http://identifiers.org/hco/5/GRCh38#145939797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42188666-C-A

145940451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42189299-C-G

145940536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42189348-G-A

145940536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42189348-G-T

145940612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42189425-T-G

145940662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42189473-T-G

145941024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42189826-G-A

http://identifiers.org/hco/5/GRCh38#145941547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42190321-C-A

145941567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42190341-A-T

http://identifiers.org/hco/5/GRCh38#145941588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42190362-C-A

145941588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42190362-C-T

145941863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42190588-G-C

145941994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42190706-G-C

145942038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42190751-G-A

145942324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42191039-C-G

http://identifiers.org/hco/5/GRCh38#145942399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42191096-A-C

http://identifiers.org/hco/5/GRCh38#145942437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42191133-C-A

145942595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42191319-T-A

145942682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42191397-G-A

145942768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42191488-C-G

145942853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42191574-C-T

145943004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42191721-G-C

http://identifiers.org/hco/5/GRCh38#145944022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#42193034-A-C

145944218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42193235-G-A

145944218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42193235-G-T

145944284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42193283-C-G

145945097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42193843-G-T

145945170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42193916-A-G

145945195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42193941-A-G

145945474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42194192-A-G

145945754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42194441-C-T

145945755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42194442-G-A

145945755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42194442-G-C

145946121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42194783-C-T

145946192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42194837-G-A

145946656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42195269-C-T

145946665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42195278-C-T

145946928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42195518-G-T

145948519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42198106-C-G

145948519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42198106-C-T

145948702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42198321-A-G

145948800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42198421-G-C

http://identifiers.org/hco/5/GRCh38#145948983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42198570-C-A

145949047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42198676-T-C

145949161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42198782-C-T

145949244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42198971-C-T

145949314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42199036-C-T

145949696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42199398-C-T

145949936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42199753-G-A

145949997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42199804-C-T

145950179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200018-C-G

145950307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200168-G-A

145950899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200720-G-A

145950967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200821-T-C

145951011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200863-C-T

145951758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42201962-G-A

145951895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42202348-G-C

145952013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42202419-T-G

http://identifiers.org/hco/5/GRCh38#145952031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42202434-A-C

145952125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42202509-G-T

145952224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42202611-G-A

145952541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203478-T-A

145952541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203478-T-G

145952748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203677-G-A

145952784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203712-T-C

145952932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203839-A-G

145953043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203948-T-C

145958381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206834-T-C

145958381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206834-T-G

145958444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206891-A-G

145958573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207012-G-T

145958720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207570-C-T

145958843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207677-C-G

145958890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207712-C-T

145959001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207797-A-T

145959126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207904-A-G

145959254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208043-G-A

145959489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208266-C-G

145959489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208266-C-T

145959497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208274-T-C

145959504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208281-C-T

http://identifiers.org/hco/5/GRCh38#145959594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42208383-A-C

http://identifiers.org/hco/5/GRCh38#145959767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42208486-C-A

http://identifiers.org/hco/5/GRCh38#145959798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42208519-C-A

145959809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208530-G-T

145959832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208576-G-A

145959846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208589-A-G

145959987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208716-G-A

145959987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208716-G-T

145960698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209466-G-A

145960699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209469-G-A

145960702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209472-G-A

145960702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209472-G-T

145960708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209478-G-C

145960785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209554-A-G

145960824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209593-G-A

145960824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209593-G-C

145960824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209593-G-T

145961529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210252-C-T

145961598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210325-G-C

145962125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211042-A-G

145962410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211304-A-G

145962436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211314-C-G

145962530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211386-G-A

145962623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211486-C-G

145963230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42212828-T-G

http://identifiers.org/hco/5/GRCh38#145964630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42213354-A-C

145964735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213422-T-G

145964765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213451-G-C

145964819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213505-T-C

145964857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213541-C-T

145965346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213712-G-A

145965368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213718-G-A

145965448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213800-C-T

145965517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213866-G-A

145965547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213896-A-G

145965549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213898-T-G

145965666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42214015-C-T

145965857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42214434-T-A

145966041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42214624-T-C

145966054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42214637-C-T

145966096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42214672-T-C

145966281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42214792-G-A

145966281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42214792-G-C

145967189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215271-G-A

145967196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215279-C-G

145967371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215763-G-A

145967433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215826-G-T

145967594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215989-A-G

145968708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42216575-T-A

145968797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42216645-A-G

145971187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42217620-C-T

145971248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42217682-G-A

145974048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42218910-G-C

http://identifiers.org/hco/5/GRCh38#145974394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42219249-C-A

145974781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42219602-G-A

http://identifiers.org/hco/5/GRCh38#145975096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42220112-C-A

145975099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220114-G-A

145975115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220130-T-G

145975120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220135-T-A

145975764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42220755-A-G

145975838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42220838-C-T

145975856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220856-G-A

145975926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42220932-A-G

145977779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42221030-C-T

145977789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42221040-T-C

145977890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42221133-A-G

145978056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42221571-G-A

145978934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222560-G-A

145979120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222701-A-G

145979294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222839-G-A

145979351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42222894-C-T

145979412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222957-A-G

145979966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42223536-C-T

145981437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42224187-T-A

145981437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42224187-T-C

145981481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42224231-T-A

145981481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42224231-T-C

145981528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42224279-T-A

145981729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42224464-T-A

145981729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42224464-T-C

145981875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42224572-A-G

http://identifiers.org/hco/5/GRCh38#145982204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42224868-C-A

http://identifiers.org/hco/5/GRCh38#145982337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42224973-C-A

145982616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42225497-A-G

145982715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42225587-A-G

145982860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42225703-A-G

145983029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226059-A-G

145983029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226059-A-T

145983034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226064-T-C

145983047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226077-G-A

145983199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226217-A-G

145983332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226303-C-T

145983349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226320-C-T

145983459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226418-G-A

http://identifiers.org/hco/5/GRCh38#145983494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42226465-C-A

145983538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226509-A-T

145983989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226956-G-A

145983989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42226956-G-T

145984135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42227093-G-A

145984235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42227195-C-T

145984336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42227285-A-T

145985473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42227613-C-G

145985473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42227613-C-T

145985475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42227615-A-G

145986170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42227950-G-A

145986170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42227950-G-T

145986357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42228185-T-G

http://identifiers.org/hco/5/GRCh38#145986411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42228236-C-A

145986862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42228689-C-G

145986871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42228698-C-T

145986878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42228705-G-A

145986895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42228722-C-T

145987244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42228969-C-G

145987249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42228974-G-A

145987659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42229098-G-A

145987660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42229099-A-G

145987934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42229390-A-G

145987963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42229417-T-G

145988055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42229482-G-A

145990820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42229575-C-T

145990823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42229577-G-A

145991635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42230382-T-A

145991735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42230482-T-C

145991911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42230646-A-G

145995028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42231372-C-T

145995122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42231426-T-C

145995232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42231534-G-A

145995232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42231534-G-C

145995232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42231534-G-T

145995292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42231590-G-C

145995292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42231590-G-T

145995353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42231643-G-A

145995517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42231777-A-G

http://identifiers.org/hco/5/GRCh38#145996080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42232258-A-C

http://identifiers.org/hco/5/GRCh38#145996155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42232312-A-C

145996382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42232501-G-A

146000143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 42234682-G-A

146000192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 42234731-C-G

146000192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42234731-C-T

146000195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42234734-G-A

146000398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42234918-T-C

146000433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42234944-A-G

146000474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42234969-T-A

146001406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42235324-T-G

146001438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42235356-T-C

http://identifiers.org/hco/5/GRCh38#146001596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42235509-A-C

146001596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42235509-A-G

146003422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42236627-A-G

146003445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42236643-T-C

146003581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42236761-A-G

146003644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42236824-T-C

http://identifiers.org/hco/5/GRCh38#146003886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42236982-C-A

http://identifiers.org/hco/5/GRCh38#146003936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42237019-A-C

146003936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237019-A-G

146003936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237019-A-T

http://identifiers.org/hco/5/GRCh38#146003957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42237033-C-A

http://identifiers.org/hco/5/GRCh38#146003997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42237068-C-A

146004162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237231-G-C

146004219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237281-G-A

146004219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237281-G-T

146004247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237309-G-A

146004247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237309-G-T

146004272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237329-C-G

http://identifiers.org/hco/5/GRCh38#146004300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42237358-A-C

146004300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237358-A-G

146004329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237385-G-A

146004497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237573-G-A

146004497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237573-G-T

146004569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237633-T-C

146004710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42237954-A-G

146005060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42238312-A-G

146005173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42238612-A-G

146005640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42239074-C-T

http://identifiers.org/hco/5/GRCh38#146005809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42239230-A-C

146005848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42239264-T-A

146005900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42239332-T-A

146005948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42239401-C-T

146007084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42240133-T-C

146007094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42240143-T-C

146007293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42240538-C-T

146007424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42240685-G-A

146007563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42240796-T-C

146007580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42240813-A-T

146007590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42240823-A-G

http://identifiers.org/hco/5/GRCh38#146007593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42240826-A-C

146007664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42240899-C-T

146007685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42240920-G-C

146008084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241294-C-G

146008256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42241455-A-G

146008286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241485-G-A

146008306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241503-G-A

146008342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241556-G-A

146008393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241613-C-G

146008393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241613-C-T

146008415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241632-T-C

146008744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241937-A-G

146008765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241958-C-T

146008806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42241998-G-A

146008871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42242061-G-T

146009059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42242407-T-G

146009208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42242685-A-G

146009510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42242914-G-T

146009569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42242971-G-A

146009588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42242997-G-A

146009588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42242997-G-C

146009609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42243018-C-G

146009729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42243323-T-C

146009796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42243404-T-C

146009812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42243420-T-A

146012841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42243739-G-A

146013619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42244070-G-A

146013619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42244070-G-T

146013758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42244195-C-T

http://identifiers.org/hco/5/GRCh38#146013854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42244297-C-A

146013854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42244297-C-T

146013878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42244321-G-A

146014053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 42244496-G-A

146014156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42244592-G-A

146014167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42244603-G-A

146014167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42244603-G-T

146014295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42244728-G-A

146014606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245149-T-C

146014637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245180-G-A

146014662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245204-T-C

146014927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245477-A-G

146014933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245483-T-C

146014991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245542-A-G

146015289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245836-C-T

146015291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245838-C-T

http://identifiers.org/hco/5/GRCh38#146015445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42245997-C-A

146015753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42246304-C-T

146015817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42246349-G-A

146016127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42246731-G-C

146016245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42246827-A-G

146016594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42247700-G-T

http://identifiers.org/hco/5/GRCh38#146016694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42247771-C-A

146017338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42250138-G-C

146017361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42250169-T-C

146017728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42250515-A-G

146017816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42250589-C-T

146018055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42250857-G-A

146020257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42250977-C-T

http://identifiers.org/hco/5/GRCh38#146020574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42251470-A-C

146020574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42251470-A-G

146021104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42251958-A-G

146021942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42252389-C-T

146023936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42253246-G-C

146024100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42253428-T-C

http://identifiers.org/hco/5/GRCh38#146024315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42253778-C-A

146024742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42254166-G-T

146024967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42254392-T-C

146024981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42254407-G-A

146024981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42254407-G-T

146025033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42254448-C-T

146025406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42254832-C-T

146025670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42255105-A-T

146026288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42255590-G-T

146026325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42255627-G-A

146026391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42255671-A-G

146026660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42255943-G-A

http://identifiers.org/hco/5/GRCh38#146026795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42256051-C-A

146026933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256111-C-T

146026960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256138-T-C

146026975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256147-A-T

146027004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256176-C-T

146027191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256362-C-T

146027303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256502-G-A

146027465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256728-G-A

146027874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42257103-A-G

146027961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42257198-C-T

http://identifiers.org/hco/5/GRCh38#146028629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42257449-C-A

146029177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42257881-A-T

146029399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42258063-C-T

146029582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42258231-G-C

146029958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42258571-T-C

146030013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42258625-C-T

146030268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42258844-G-A

146030301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42258870-A-G

146030588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259105-T-C

146031017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259465-T-C

146031089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259537-G-A

146031216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259640-T-C

146031272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259697-C-T

146031430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259861-C-T

146031513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260069-T-C

146031621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260187-A-G

146031639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260205-A-T

146031713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260275-A-T

146031878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260428-C-T

146031931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260473-C-T

146032129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260663-A-G

146032189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260721-G-A

146032599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42261341-G-A

146032599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42261341-G-C

http://identifiers.org/hco/5/GRCh38#146032615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42261350-C-A

146032615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42261350-C-T

146032760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42261438-A-G

http://identifiers.org/hco/5/GRCh38#146032888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42261559-C-A

146032975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42261647-G-C

146033190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262261-G-T

146033348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262420-T-A

146033363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262449-A-T

146034107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262855-C-T

http://identifiers.org/hco/5/GRCh38#146034143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42262890-C-A

146034197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262940-A-T

146034429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42263155-C-T

146034478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42263205-A-G

146034565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42263294-C-T

146035154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42263653-G-A

146035300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42263819-C-G

http://identifiers.org/hco/5/GRCh38#146035401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42263909-C-A

146035730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265050-G-A

146035740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265061-C-T

146035741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265062-A-G

146035791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265112-C-T

146035805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265125-G-C

http://identifiers.org/hco/5/GRCh38#146035902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42265220-A-C

146035979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265281-G-A

146035979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265281-G-C

146036861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265445-C-T

146036915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265491-C-T

146037088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265663-T-G

146037091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42265666-A-G

146047207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272067-G-A

146047429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272264-G-T

146047602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272424-C-T

http://identifiers.org/hco/5/GRCh38#146047683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42272503-C-A

146047683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272503-C-T

146047716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272527-G-A

146047820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42272631-G-A

146047820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42272631-G-C

146047914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272708-C-T

146047975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272756-T-A

146047975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272756-T-C

146047977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272758-G-A

146047977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272758-G-T

http://identifiers.org/hco/5/GRCh38#146047987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42272768-C-A

http://identifiers.org/hco/5/GRCh38#146047999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42272782-C-A

146047999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272782-C-G

146047999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272782-C-T

146048011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272794-T-A

146048011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272794-T-C

146048802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42273384-G-A

146049038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42273961-T-A

http://identifiers.org/hco/5/GRCh38#146049316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42274195-C-A

146049316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42274195-C-G

146049560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42274527-C-T

146049634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42274601-T-C

146049663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42274630-G-A

146049960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42274896-T-C

146050043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42274956-G-T

146050312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42275130-G-A

146050434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42275287-G-A

146050440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42275293-A-G

http://identifiers.org/hco/5/GRCh38#146050468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42275321-C-A

146051271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276049-G-A

146051431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276211-A-G

146051436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276214-C-G

146051436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276214-C-T

146051679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276459-G-A

146051840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276616-G-C

146051860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276634-T-C

146052042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276815-C-T

146052258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277046-G-A

146052696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277439-T-A

146052696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277439-T-G

146052707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277450-T-C

146052730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277473-C-T

146052777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277518-T-C

http://identifiers.org/hco/5/GRCh38#146052883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42277623-C-A

146052883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277623-C-G

146052883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277623-C-T

146052897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277637-G-A

146053091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277804-A-G

146053279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42278115-A-G

146053279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42278115-A-T

146053693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42279067-T-C

146054290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42279634-T-C

146054321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42279665-A-G

146054404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42279749-C-G

http://identifiers.org/hco/5/GRCh38#146054416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42279761-C-A

146054516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42279857-C-T

146054566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42279898-G-A

146054702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42280034-C-T

146054805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42280135-A-G

146054945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42280275-A-G

146055045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42280373-C-G

146055317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42280644-G-T

146055340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281048-T-C

146055655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281333-T-C

146055711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281384-G-A

146055711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281384-G-T

http://identifiers.org/hco/5/GRCh38#146055717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42281390-C-A

146055717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281390-C-G

146055747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281417-A-G

http://identifiers.org/hco/5/GRCh38#146055773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42281439-C-A

146055773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281439-C-T

http://identifiers.org/hco/5/GRCh38#146055775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42281441-C-A

146055775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281441-C-T

http://identifiers.org/hco/5/GRCh38#146055781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42281447-C-A

146055805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281471-G-A

146055805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281471-G-T

http://identifiers.org/hco/5/GRCh38#146055832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42281497-C-A

146056088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42282795-G-A

http://identifiers.org/hco/5/GRCh38#146056110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42282817-C-A

146056110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42282817-C-T

146056237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42282948-T-C

146056237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42282948-T-G

146056252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42282962-G-A

http://identifiers.org/hco/5/GRCh38#146056306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42283012-C-A

146056306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283012-C-G

146056358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283057-G-A

http://identifiers.org/hco/5/GRCh38#146056446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42283144-C-A

146056486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283182-A-G

http://identifiers.org/hco/5/GRCh38#146056489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42283185-C-A

146056610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283272-G-A

146056610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283272-G-T

146056612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283274-C-T

146056816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283446-A-T

http://identifiers.org/hco/5/GRCh38#146056865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42283490-A-C

146056883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283508-T-C

146056901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283527-C-G

146056949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283577-A-T

146057284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283950-C-G

146057284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283950-C-T

146057343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284000-C-G

146057371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284025-A-G

146057414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284047-C-T

http://identifiers.org/hco/5/GRCh38#146057527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42284126-C-A

146057678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284253-A-G

146057740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284334-G-T

146057767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284361-T-C

146058028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284538-C-T

146058126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284637-G-T

146058296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284802-G-A

146058404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284885-C-T

http://identifiers.org/hco/5/GRCh38#146058427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42284908-A-C

146058474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284984-G-T

146058501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42285020-C-T

146058553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42285094-A-G

146058636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42285178-T-C

146059740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42285964-T-C

146059754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42285978-T-G

146059848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42286064-T-C

146059886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42286102-C-G

146059886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42286102-C-T

146059894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42286110-C-G

146059894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42286110-C-T

146059950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42286166-G-A

146060309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42286657-G-A

146060309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42286657-G-C

146060309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42286657-G-T

http://identifiers.org/hco/5/GRCh38#146060328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42286678-C-A

146060328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42286678-C-T

http://identifiers.org/hco/5/GRCh38#146060331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42286681-C-A

146060352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42286703-T-C

http://identifiers.org/hco/5/GRCh38#146060739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42287286-C-A

146060766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287313-A-G

146060938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287465-T-C

http://identifiers.org/hco/5/GRCh38#146061050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42287576-C-A

146061050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287576-C-T

146061051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287577-G-A

http://identifiers.org/hco/5/GRCh38#146061068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42287594-C-A

146061068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287594-C-T

146061069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287595-G-A

146061082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287608-G-A

146061090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287616-C-T

146061091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287617-A-T

146061240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287766-G-A

146061304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287813-T-C

146061442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42287952-A-G

146061661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288210-T-C

146061674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288224-T-C

146061854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288547-G-C

146061867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288560-A-G

146062079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288745-A-G

146062224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288823-C-G

146062335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288906-A-G

146062335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288906-A-T

146062401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288993-C-T

146062506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42289097-T-G

146062554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42289145-G-A

146062585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 42289176-C-T

146062656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42289247-G-A

146062656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42289247-G-T

146062686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42289277-G-A

146062797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289387-G-A

146062797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289387-G-T

http://identifiers.org/hco/5/GRCh38#146062966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42289646-C-A

146062995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289675-G-A

146062995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289675-G-T

146063025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289702-G-A

146063025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289702-G-T

146063091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289762-C-T

146063202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289857-A-T

146063211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289866-G-T

146063230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289885-T-A

146063230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289885-T-G

146063281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42289937-T-C

http://identifiers.org/hco/5/GRCh38#146063381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42290036-C-A

146063456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42290112-A-G

146064129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42290337-A-G

http://identifiers.org/hco/5/GRCh38#146064922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42290791-C-A

146064922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42290791-C-T

http://identifiers.org/hco/5/GRCh38#146065060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42290924-C-A

146065330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291122-G-T

146065431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291215-T-C

146065472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291256-G-A

146065722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291457-T-A

146065742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291477-G-C

146065781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291514-G-A

146066003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291590-T-C

146066006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291593-T-A

146066674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292402-A-G

146066922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292623-A-G

146067033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292716-T-G

http://identifiers.org/hco/5/GRCh38#146067093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42292764-A-C

146067228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42292882-T-C

146067354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42293010-G-A

146067354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42293010-G-C

146067367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42293021-G-A

146067411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42293066-C-T

146067517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42293165-G-T

146067545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42293193-G-A

146067813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42293452-C-T

146067871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42293497-C-T

146067980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42293601-T-C

146068348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42293927-T-C

http://identifiers.org/hco/5/GRCh38#146068873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42294581-A-C

146069015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42294691-C-G

http://identifiers.org/hco/5/GRCh38#146069019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42294695-C-A

146069031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42294708-A-G

146069031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42294708-A-T

http://identifiers.org/hco/5/GRCh38#146069087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42294764-A-C

146070110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42295464-G-C

146070235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42295604-A-G

146070319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42295709-G-A

146070614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42295979-T-A

146070614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42295979-T-C

146070649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42296014-G-A

http://identifiers.org/hco/5/GRCh38#146070716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42296075-A-C

146070907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42296239-T-C

http://identifiers.org/hco/5/GRCh38#146070978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42296310-C-A

146070978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42296310-C-G

146070978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42296310-C-T

146071021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42296352-T-A

146071118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42296453-C-T

146072921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42296539-T-C

146073087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42296705-G-A

146073638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42297181-G-A

146073777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42297226-G-C

146074060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42297496-G-A

146074060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42297496-G-T

146074076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42297512-G-T

146074371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42297718-G-T

146074514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42297875-G-A

146074819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42298237-C-T

http://identifiers.org/hco/5/GRCh38#146074823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42298241-A-C

146074851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42298285-C-G

http://identifiers.org/hco/5/GRCh38#146075091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42298515-C-A

146075385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42298803-C-T

146075959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42299003-T-C

146076162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42299188-C-T

146076178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42299204-A-G

146076204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42299230-G-A

146076230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, undefined
orthologous variants: 42299255-T-A

http://identifiers.org/hco/5/GRCh38#146076236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#42299261-C-A

146076236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron_variant, undefined
orthologous variants: 42299261-C-T

146076253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42299278-G-A

146076253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42299278-G-C

http://identifiers.org/hco/5/GRCh38#146076436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42299462-C-A

146076436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42299462-C-T

146076437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42299463-G-A

146076860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42300118-A-G

146076861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42300119-C-T

146077045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42300298-C-G

146077210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42300500-A-G

146077331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42300612-T-C

http://identifiers.org/hco/5/GRCh38#146077474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42300752-A-C

146077511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42300789-T-C

146077534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42300817-G-C

146077676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42300978-T-C

146077676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42300978-T-G

146078210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42301472-G-T

http://identifiers.org/hco/5/GRCh38#146078314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42301565-C-A

146078379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42301629-A-G

146078432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: intron variant
orthologous variants: 42301680-A-G

146078474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42301721-A-G

146078562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42301807-G-T

146078679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42301901-G-T

146078861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42302080-G-C

146078861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42302080-G-T

146078943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42302138-C-T

http://identifiers.org/hco/5/GRCh38#146078971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42302166-C-A

146078971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42302166-C-T

146079101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307221-G-C

146079383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307463-G-A

http://identifiers.org/hco/5/GRCh38#146079423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42307498-C-A

146079508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307569-G-A

146079508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307569-G-T

146079519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307580-G-A

http://identifiers.org/hco/5/GRCh38#146079601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42307666-C-A

146079601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307666-C-T

146079622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307687-A-G

146079628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307693-G-T

146079633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307698-C-T

146079644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307704-T-C

146079683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307742-G-C

146079704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307758-T-C

146079841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42307856-G-T

146080029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308115-A-G

146080072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308203-T-C

146080159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308322-T-C

146080221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308384-C-T

146080296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308457-G-A

146080296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308457-G-T

146080306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308465-A-G

http://identifiers.org/hco/5/GRCh38#146080402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42308565-C-A

http://identifiers.org/hco/5/GRCh38#146080480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42308639-A-C

146080526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308688-G-T

http://identifiers.org/hco/5/GRCh38#146080558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42308710-A-C

146080558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308710-A-G

146080642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42308799-G-T

146081315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42309311-T-C

146081347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42309343-C-T

http://identifiers.org/hco/5/GRCh38#146081372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42309369-A-C

146081483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42309472-A-G

146081500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42309487-G-A

146081500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42309487-G-T

146081501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42309488-C-T

146081553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42309534-G-C

146081553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42309534-G-T

146081632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26299
most severe consequence: 3 prime UTR variant
orthologous variants: 42309619-C-T