38687104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564758-C-T

38687105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564757-G-T

38687111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564751-G-A

38687111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564751-G-T

38687114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564748-G-A

38687114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564748-G-T

38687118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564744-G-A

38687118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564744-G-C

38687118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564744-G-T

http://identifiers.org/hco/13/GRCh38#38687142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53564728-A-C

38687142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564728-A-G

38687149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564721-G-C

38687174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564695-G-A

38687174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564695-G-C

38687174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564695-G-T

38687281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53564589-G-T

http://identifiers.org/hco/13/GRCh38#38687415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53564451-C-A

http://identifiers.org/hco/13/GRCh38#38687725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53564144-C-A

38687725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53564144-C-G

http://identifiers.org/hco/13/GRCh38#38687933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53563936-A-C

38687933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563936-A-G

http://identifiers.org/hco/13/GRCh38#38687947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53563922-C-A

38687947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53563922-C-T

38688035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563834-G-A

http://identifiers.org/hco/13/GRCh38#38688061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53563808-C-A

38688061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53563808-C-G

38688061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53563808-C-T

38688062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563807-C-T

38688073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53563796-C-T

38688090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563779-C-T

38688213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563656-G-A

38688234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563635-C-T

http://identifiers.org/hco/13/GRCh38#38688269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53563600-A-C

38688269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563600-A-G

38688290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563579-A-T

38688332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563537-G-A

38688461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563408-A-G

38688479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563390-C-G

38688561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563308-G-A

38688561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563308-G-T

38688723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563146-C-T

38688858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53563011-A-G

http://identifiers.org/hco/13/GRCh38#38688913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53562956-C-A

38688913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562956-C-G

38688913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53562956-C-T

38688953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562916-G-T

38689076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562793-C-T

38689139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562730-G-A

38689143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562726-T-A

38689148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562721-T-G

38689191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562678-A-G

38689201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53562668-T-C

38689316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562565-T-A

38689316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562565-T-C

http://identifiers.org/hco/13/GRCh38#38689418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53562463-C-A

38689418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562463-C-G

38689418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562463-C-T

38689463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562418-T-G

http://identifiers.org/hco/13/GRCh38#38689583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53562298-A-C

38689583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562298-A-G

38689583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562298-A-T

http://identifiers.org/hco/13/GRCh38#38689603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53562278-C-A

38689603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562278-C-G

38689856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53562025-A-G

38689919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53561962-A-G

38690111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53561770-C-T

38690155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53561726-T-C

38690207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53561674-G-A

38690405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53561476-G-A

38690489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53561392-A-G

38690675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53561206-A-G

38690729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53561152-G-A

38690827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53561054-C-G

38690827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53561054-C-T

38690933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 53560948-G-T

38690939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560942-A-G

38690984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560897-A-G

38691026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560855-A-G

38691107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560774-G-A

38691107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560774-G-T

http://identifiers.org/hco/13/GRCh38#38691182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53560699-A-C

38691182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560699-A-G

38691203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560678-T-A

38691203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560678-T-C

38691221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560660-C-T

38691335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560546-G-T

38691421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53560460-T-A

38691461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560420-G-A

http://identifiers.org/hco/13/GRCh38#38691469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53560412-A-C

38691533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560348-G-T

38691611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560270-G-A

38691707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53560174-A-T

http://identifiers.org/hco/13/GRCh38#38691878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53560003-A-C

38691911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53559970-C-G

38691911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53559970-C-T

38691926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53559955-G-A

38691926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53559955-G-T

38692010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53559871-C-G

38692040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53559841-A-G

http://identifiers.org/hco/13/GRCh38#38692316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53559565-A-C

http://identifiers.org/hco/13/GRCh38#38692502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53559379-A-C

38692502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53559379-A-G

38692545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53559326-A-G

38692545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53559326-A-T

38692548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53559323-C-T

38692650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53558929-G-A

38692650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53558929-G-T

38692810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53558773-C-G

38693044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53558544-T-C

38693170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53558413-G-A

38693170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53558413-G-C

38693170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53558413-G-T

38693229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53558354-A-G

38693265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53558311-T-C

38693471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53557989-T-A

http://identifiers.org/hco/13/GRCh38#38693892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53557587-C-A

38693968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53557521-C-T

38694080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53557402-T-A

38694237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53557252-A-G

38694284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53557205-G-A

38694583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53556920-A-G

http://identifiers.org/hco/13/GRCh38#38694662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53556860-C-A

38694775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53556749-A-G

38694777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53556747-T-G

38694785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53556739-A-G

38696503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53556417-A-G

38696556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53556369-C-T

38697447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53555639-G-A

38697601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53555492-A-G

38697607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53555487-A-G

38697608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53555486-T-C

38697610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53555484-G-C

38697838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53555254-G-C

38697838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53555254-G-T

38698320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53555094-G-A

38698320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53555094-G-T

38698565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554851-C-T

38698704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554717-A-T

38698874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554564-T-C

38698989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554452-A-G

38699006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554435-A-G

38699012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53554429-A-T

38699277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553754-C-G

38699312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553723-T-C

38699319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553716-C-T

38699747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553307-C-G

38699749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553305-A-G

38699806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553238-T-G

38699817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553227-G-A

http://identifiers.org/hco/13/GRCh38#38699819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53553208-A-C

38699819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553208-A-G

38699819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553208-A-T

38699864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553151-G-C

38699927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553079-T-C

http://identifiers.org/hco/13/GRCh38#38699928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53553078-C-A

38699931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53553075-T-C

38700708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53545181-G-T

38700729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53545159-T-C

38701567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53544973-C-G

38701611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53544923-T-G

38701999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53544538-G-A

http://identifiers.org/hco/13/GRCh38#38702159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53544379-A-C

38702226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53544321-C-T

38702266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53544284-C-T

38702307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53544238-A-T

38702497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53544057-G-A

38702505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53544049-A-G

38702544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53543982-G-C

38702544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53543982-G-T

38702577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53543949-T-G

38703288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53543178-T-C

38703339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53543128-A-T

38703490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53542987-C-G

38703512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53542966-C-T

38703724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53542795-T-G

38703854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53542678-T-C

38703966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53542560-T-A

38704029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53542506-G-A

38704149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53542387-G-C

38704149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53542387-G-T

38705325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53541437-A-G

38705371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53541400-C-G

38705384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53541389-A-T

38705461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53541316-C-G

38705509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53541285-T-G

38705772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53541034-C-T

38705911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53540726-A-G

38706068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53540588-G-A

38706553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539940-G-A

38706603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539906-C-T

38706735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539793-G-A

38706817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539718-T-A

38706999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539394-C-G

38707102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539290-C-T

38707130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53539194-C-T

38707472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53538866-G-C

38707785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53538580-C-G

http://identifiers.org/hco/13/GRCh38#38707823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53538551-A-C

38707999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53538387-T-C

38708031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53538366-A-G

38708134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53538271-G-A

38708218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53538188-G-C

38708739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537973-T-C

38709300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537533-G-A

38709300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537533-G-T

38709361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537481-T-C

38709365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537477-G-A

38709370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537472-A-G

38709418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537423-T-G

38709459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537382-A-G

38709566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537288-A-G

http://identifiers.org/hco/13/GRCh38#38709605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53537254-A-C

http://identifiers.org/hco/13/GRCh38#38709728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53537138-A-C

http://identifiers.org/hco/13/GRCh38#38709776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53537114-C-A

38709785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53537093-G-T

38711038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53536455-A-G

38711050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53536443-T-C

38711325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53536167-A-G

38711325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53536167-A-T

38711398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53536090-C-T

38711507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535987-T-A

38716352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535722-T-C

38716443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535629-A-G

38716456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535616-A-G

38717805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535413-A-G

38717809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535409-A-G

38717810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535408-A-G

38717929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535313-A-T

38718054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535195-T-G

38718058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53535191-T-C

38718186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53534655-A-G

38718237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53534604-A-G

38718338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53534507-G-A

38718394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53534450-T-C

38718396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53534448-G-A

http://identifiers.org/hco/13/GRCh38#38718549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53534301-C-A

38718549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53534301-C-T

38719567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532687-C-G

38719567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532687-C-T

http://identifiers.org/hco/13/GRCh38#38719585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53532669-A-C

38719606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532649-T-C

38719610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532645-C-T

38719790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532464-T-A

38720069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532215-G-C

38720185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532078-T-G

38720255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53532030-A-G

38720294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53531992-T-C

38720317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53531969-G-A

38720717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53531785-G-A

38720852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53531718-G-A

38721621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

38726098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53529106-C-T

38726233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528991-C-T

38726243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528982-G-A

http://identifiers.org/hco/13/GRCh38#38726247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53528978-C-A

38726424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528868-T-C

38726526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528776-C-T

38726626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528724-T-A

38726745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528612-C-T

38726777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528581-A-G

38726777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528581-A-T

38726811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528547-T-C

38726879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528491-G-C

38727015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528356-T-C

38727036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528335-G-A

38727135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528233-G-A

http://identifiers.org/hco/13/GRCh38#38727224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53528148-C-A

38727526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53528094-C-T

38727764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53527892-T-G

38727908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53527745-T-G

38728050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53527622-G-A

38729606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53526159-A-G

38729932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53525386-A-G

38729967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53525379-T-C

38730429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53524961-G-A

38730493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53524889-G-C

38730809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53524544-T-A

38730979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53524219-T-C

38731475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53523770-A-G

38731479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53523766-A-G

38731621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53523613-C-T

38731623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53523611-A-T

38732438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53522965-G-C

http://identifiers.org/hco/13/GRCh38#38732548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53522855-A-C

38732920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53522482-G-C

38733991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53520413-A-G

38735194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53519318-T-A

38735237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53519275-T-A

38735237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53519275-T-C

38735276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53519238-C-T

38735629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518917-G-A

38735629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518917-G-T

38735697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518852-A-G

38735699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518850-A-G

38735770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518788-A-G

38735901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518700-A-G

38735910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518691-C-G

38736016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518607-G-A

38736264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518379-C-T

38736329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53518314-T-C

38736606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53517967-T-C

38736673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53517899-A-G

http://identifiers.org/hco/13/GRCh38#38736693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53517884-A-C

38736744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53517835-A-G

38737138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53517421-T-C

38737291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53517283-G-A

38737610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53514607-C-T

38737621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53514596-G-T

38737716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53514509-C-T

38737820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53514447-T-C

38738071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53514216-A-G

38740074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53512689-A-G

38740143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53512622-C-T

38740151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53512614-G-C

http://identifiers.org/hco/13/GRCh38#38740569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53512223-C-A

38740712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53512080-T-C

38740714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53512078-G-A

38748897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510566-G-A

38748897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510566-G-T

38748933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510438-G-A

http://identifiers.org/hco/13/GRCh38#38749232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53510168-A-C

38749346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510054-A-G

38749402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53510008-T-C

38752005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53507941-G-A

38752005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53507941-G-C

38752294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53507690-A-G

38752373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53507348-G-C

38752584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53507182-G-A

http://identifiers.org/hco/13/GRCh38#38752835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53506996-C-A

38752851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53506980-G-A

38752960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53506879-C-T

38753278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53506524-T-C

38753358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53506465-G-A

38753412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53506392-T-C

http://identifiers.org/hco/13/GRCh38#38753423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53506382-C-A

38753423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53506382-C-G

38753487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53506320-T-C

38753935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505904-G-T

38754063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505790-G-C

38754063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505790-G-T

38754112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505755-G-A

38754116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505751-G-A

38754145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505724-G-A

http://identifiers.org/hco/13/GRCh38#38754244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53505627-C-A

38754244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505627-C-T

38754499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505215-A-G

38754507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505207-T-A

38754577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53505166-A-G

38758584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502193-C-T

38758661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53502116-G-A

38758825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501954-A-G

38758848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501935-C-T

38759393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501511-C-T

38759404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501500-G-C

38759418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501486-G-A

38759470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501441-T-A

38759689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501227-A-G

38759759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501159-C-T

38759797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501123-C-T

38759799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501121-G-C

38759822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501098-G-T

38759862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53501060-G-A

38760146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53500858-T-C

http://identifiers.org/hco/13/GRCh38#38760766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53500277-A-C

38762916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498678-C-T

38763011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498572-T-C

38763022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498561-T-A

38763028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498555-A-G

38763112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53498473-C-T

38763221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498374-T-C

38763349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498258-T-C

38763352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498255-T-G

http://identifiers.org/hco/13/GRCh38#38763478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53498120-A-C

38763478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498120-A-G

38763478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498120-A-T

http://identifiers.org/hco/13/GRCh38#38763500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53498090-A-C

38763500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53498090-A-T

38764136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53497437-A-G

38764318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53497266-A-G

38764413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53497171-T-C

38764535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53497065-A-G

38764537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53497063-T-C

http://identifiers.org/hco/13/GRCh38#38764539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53497061-C-A

http://identifiers.org/hco/13/GRCh38#38764573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53497020-C-A

38764985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53496726-A-G

http://identifiers.org/hco/13/GRCh38#38764986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53496725-C-A

38765567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53496299-A-G

38765719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53496220-T-C

38765733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53496158-T-C

38765787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53496076-T-C

38765858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53496011-A-T

38765877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53495992-G-A

38765973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53495888-A-G

38766065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53495800-G-A

38766068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53495797-T-G

38766155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53495719-A-G

38766195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53495679-A-T

http://identifiers.org/hco/13/GRCh38#38766455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53495418-A-C

38766838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53494302-A-G

38766958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53494176-A-G

38766958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53494176-A-T

38767155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53494008-T-C

38767170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493989-C-T

38767776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493502-A-G

38768035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53493261-T-C

38769601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53493112-G-A

http://identifiers.org/hco/13/GRCh38#38769655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53493058-C-A

38769715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53492998-T-C

38769802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53492911-G-A

38769832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492881-T-G

38770658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492533-C-T

38770804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492393-A-G

38770928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492272-A-G

38771091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492097-A-G

38771101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492087-A-G

http://identifiers.org/hco/13/GRCh38#38771113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53492075-A-C

38771135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492053-C-T

38771142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492046-C-G

38771157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53492031-C-G

38771217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53491971-G-T

38773842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490339-A-G

38773923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490253-T-G

38773947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490229-T-G

38774177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53490033-A-T

38774244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489989-A-G

38774608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489451-C-T

38774621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489441-C-G

38774621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489441-C-T

38774630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489432-G-A

38774846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489156-G-C

38774876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489129-C-T

38774959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53489060-G-A

38775972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488755-T-C

38776171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488555-G-A

38776263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488473-G-A

38776413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488333-G-C

38776682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488090-A-G

38776719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488052-G-C

38776721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53488050-G-A

http://identifiers.org/hco/13/GRCh38#38776780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53487993-C-A

38776780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487993-C-T

38776989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487824-A-G

38776994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487819-T-A

38777034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487784-C-T

http://identifiers.org/hco/13/GRCh38#38777126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53487575-C-A

38777126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487575-C-T

http://identifiers.org/hco/13/GRCh38#38777478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53487203-C-A

38777514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53487157-G-A

38777939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486723-C-G

38777939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486723-C-T

38778105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486557-A-G

38778302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486350-G-T

38778569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486150-T-C

38778570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486149-C-T

38778829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53486029-T-C

38781011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53484100-T-C

38781011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53484100-T-G

38781099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53484010-T-G

38781120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483992-C-T

38781135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483978-T-A

38781176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53483938-A-G

38782059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482984-G-A

38782481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482545-A-G

38782666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482381-G-A

38782792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482289-G-A

38782798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482284-G-A

http://identifiers.org/hco/13/GRCh38#38782942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53482214-A-C

38782942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53482214-A-T

http://identifiers.org/hco/13/GRCh38#38782983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53482176-C-A

38783200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53481944-C-G

38784134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480629-C-G

38784201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480564-G-A

38784519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53480116-T-C

38784539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479973-A-G

38784694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53479818-T-C

38784757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53479755-G-A

38784800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53479712-A-G

38784850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479677-T-G

38784907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479636-A-G

38784907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479636-A-T

38785083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479519-T-C

38785181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479442-C-T

http://identifiers.org/hco/13/GRCh38#38785202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53479421-C-A

38785338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479296-C-T

38785404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479264-A-G

38785433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479201-G-A

38785586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53479062-A-G

38786481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478530-G-A

38786723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53478280-A-G

38819311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53472253-T-G

38819385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53472180-A-T

38819464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53472101-G-T

38819511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53472066-A-G

38819532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53472045-A-T

38819612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471978-T-C

38819734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471807-T-A

38819813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471706-C-T

38819841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471678-T-G

38819848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471671-A-G

38819851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471668-A-G

38819999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471529-A-G

38820019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471509-A-G

38820151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471378-G-A

38820210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471323-G-A

38820217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53471316-A-G

38821422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470268-T-C

38821482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470210-C-T

38821494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470198-T-G

38821503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470189-T-C

38821593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53470070-A-T

38821672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 53469688-G-A

http://identifiers.org/hco/13/GRCh38#38821705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53469656-C-A

38821705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53469656-C-G

38821705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53469656-C-T

38821710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53469651-C-T

38821712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53469649-C-T

38821786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53469571-A-G

38821801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53469557-A-G

http://identifiers.org/hco/13/GRCh38#38821855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53469503-C-A

http://identifiers.org/hco/13/GRCh38#38821895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53469467-C-A

38821895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53469467-C-T

38821995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53469360-A-T

38822011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53469345-T-C

38822160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53469209-G-C

38822208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53469170-C-T

http://identifiers.org/hco/13/GRCh38#38822315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53469045-C-A

38822334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53469026-C-T

38822376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468995-A-T

38822493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468865-A-G

38822805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468582-G-C

38822815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468570-G-A

38822871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468512-T-C

38823083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468086-A-T

38823144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53468018-T-C

38823265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467901-T-C

38823269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467896-A-T

http://identifiers.org/hco/13/GRCh38#38823346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53467861-A-C

38823411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467799-G-A

38823414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467797-A-G

38823512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467690-C-T

http://identifiers.org/hco/13/GRCh38#38823517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53467685-C-A

38823543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467659-C-G

38823576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467630-T-G

38823594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467619-G-T

38823615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467593-T-C

38823629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467579-C-T

38825993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467246-T-G

38826083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467173-T-C

38826159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467094-A-G

38826225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53467028-G-A

38826262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466991-A-G

38826303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466942-C-T

38826368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466881-T-C

38826408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466842-C-T

http://identifiers.org/hco/13/GRCh38#38826418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53466834-C-A

38826446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466807-G-A

38826446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466807-G-C

38826523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466737-T-C

38826523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466737-T-G

38826597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466665-T-C

38826602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466660-A-G

38826637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466625-T-G

38826801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466465-A-G

38826867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466414-C-T

http://identifiers.org/hco/13/GRCh38#38826883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53466405-A-C

38826883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466405-A-G

38826899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466385-C-T

38827005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466289-C-T

http://identifiers.org/hco/13/GRCh38#38827075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53466219-C-A

38827257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53466050-A-G

38829855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465750-A-G

38830000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465610-T-C

38830002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465608-T-G

38830251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465392-T-C

http://identifiers.org/hco/13/GRCh38#38841783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53465108-A-C

38841783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465108-A-T

38841814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465076-T-C

38841853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53465032-T-C

38842106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53464900-G-A

38842149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53464857-G-T

38842402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53464616-G-A

38842517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463778-A-G

38842518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463777-T-A

38842722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463555-G-A

38842758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463519-G-A

38842810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463313-G-A

38842814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463309-G-T

38843012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463118-A-G

http://identifiers.org/hco/13/GRCh38#38843014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53463116-A-C

38843014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53463116-A-G

38843263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53462840-A-G

38843269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53462834-T-A

38843329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53462790-G-A

38843363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53462754-G-A

38843737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461433-T-A

38843737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461433-T-G

38843846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461324-C-T

38843902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461266-C-G

38843902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461266-C-T

http://identifiers.org/hco/13/GRCh38#38843947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53461213-C-A

38844047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53461120-T-G

http://identifiers.org/hco/13/GRCh38#38844507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53460815-A-C

38844843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53460481-G-C

38844941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53460385-T-G

38844947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53460379-A-G

38844995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53460325-T-G

http://identifiers.org/hco/13/GRCh38#38845159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53460180-C-A

38845159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53460180-C-T

38845269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53460039-G-A

38845422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459825-T-G

38845559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459740-T-A

38845619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459705-T-A

38845755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459587-A-G

38845927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459438-T-C

38846102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459273-C-G

38846105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459270-C-T

38846235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459139-T-A

38846241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459133-T-A

38846241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459133-T-C

38846247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53459126-T-A

38846553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458897-T-A

http://identifiers.org/hco/13/GRCh38#38846555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53458895-C-A

38846555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458895-C-T

38846576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53458876-C-G

38846614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53458838-G-A

38846626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53458826-T-G

http://identifiers.org/hco/13/GRCh38#38846656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53458796-A-C

38846706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53458746-T-G

38846707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53458745-C-G

38846745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458701-C-G

38846771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458675-G-C

38846837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458635-T-C

38846859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458609-T-C

http://identifiers.org/hco/13/GRCh38#38846865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53458601-A-C

38846865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458601-A-G

38846866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458600-G-A

38846866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458600-G-T

38846985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458495-A-G

38847074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458413-C-T

38847154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458339-A-G

38847261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458258-T-A

38847283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53458233-G-T

http://identifiers.org/hco/13/GRCh38#38848315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53457376-C-A

38848315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53457376-C-T

38848388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53457273-A-G

38848413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53457257-T-G

38848472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53457201-T-G

38848529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53457144-C-T

38848640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53457033-A-G

38848783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53456902-C-T

38848796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53456889-G-A

38848829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53456862-A-G

38848843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53456854-G-C

38849457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53456324-A-G

38849537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53455722-T-C

38849796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53455477-A-G

38849814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53455459-G-A

38849888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53455385-T-C

38849987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53455292-G-T

http://identifiers.org/hco/13/GRCh38#38849988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53455291-C-A

38849988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53455291-C-T

38849996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53455283-C-T

38850090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53455174-G-A

38850090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53455174-G-C

38850110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53455154-A-G

38850148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53455116-T-C

38850169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53455095-G-A

38850205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53455059-A-G

http://identifiers.org/hco/13/GRCh38#38850277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53454900-C-A

38850277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53454900-C-T

http://identifiers.org/hco/13/GRCh38#38850278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53454899-C-A

38850278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53454899-C-T

38850310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53454756-A-G

38850333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53454722-A-T

38850334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53454721-G-T

38850375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53454681-A-G

38850390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53454668-G-A

38850402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53454656-G-T

38850671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53453240-G-A

38850671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53453240-G-T

38850812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53453110-T-C

38850948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: synonymous variant
orthologous variants: 53452937-G-A

38851126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53452763-G-T

38851143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53452746-T-C

38851149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53452740-A-G

38851230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53452657-G-A

38851230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53452657-G-T

38851377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53452156-G-A

http://identifiers.org/hco/13/GRCh38#38851573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53451996-C-A

38851636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451937-G-A

38851661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451901-T-C

38851747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: synonymous variant
orthologous variants: 53451815-G-A

38851766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53451796-C-G

38851766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53451796-C-T

38851856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53451706-C-T

38851882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451680-A-G

38851888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451677-T-C

38851891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451674-C-T

38851897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451668-A-G

38851900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451665-G-C

http://identifiers.org/hco/13/GRCh38#38851911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53451654-C-A

38851992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451551-G-T

38853557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451073-C-T

38853601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53451030-A-G

38853646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53450990-C-T

38853699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53450968-G-A

38853745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53450950-T-A

38853841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53450851-G-A

38854105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53450604-G-C

38854241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53450494-A-G

http://identifiers.org/hco/13/GRCh38#38854261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53450482-C-A

38854273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53450470-A-G

http://identifiers.org/hco/13/GRCh38#38854302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53450425-A-C

38854366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53450375-T-G

38854490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53450276-G-A

38854749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53449932-A-G

38854937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53449779-T-C

38855336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53449384-C-T

http://identifiers.org/hco/13/GRCh38#38855353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53449293-A-C

38855376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53449207-C-G

38855535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53449034-G-A

38855945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53448661-A-G

http://identifiers.org/hco/13/GRCh38#38856030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53448593-C-A

38856030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53448593-C-T

http://identifiers.org/hco/13/GRCh38#38856042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53448581-C-A

38856042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53448581-C-G

38856042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53448581-C-T

38856079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53448566-T-A

38856079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53448566-T-C

38856158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53448488-G-A

38856158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53448488-G-T

38856194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53448452-G-C

38856194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: stop gained
orthologous variants: 53448452-G-T

http://identifiers.org/hco/13/GRCh38#38856221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53448425-C-A

38856221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53448425-C-G

38856221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: synonymous variant
orthologous variants: 53448425-C-T

38857136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53447789-G-T

38857523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53447055-C-G

38857523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53447055-C-T

38857561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53447013-T-C

38857666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446930-C-G

38857773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446833-G-A

38857773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446833-G-T

http://identifiers.org/hco/13/GRCh38#38857809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53446806-C-A

http://identifiers.org/hco/13/GRCh38#38857824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53446791-A-C

38857824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446791-A-G

38857824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446791-A-T

38858013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53446603-T-C

38858073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446543-T-C

38858154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446304-A-G

http://identifiers.org/hco/13/GRCh38#38858156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53446302-C-A

38858195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446257-C-T

38858220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446231-A-G

38858269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446184-A-G

38858349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53446099-A-G

38858608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445707-G-A

38858622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445693-A-G

38858644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445673-A-G

38858699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445601-G-C

http://identifiers.org/hco/13/GRCh38#38858801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53445491-A-C

38858833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445460-G-A

38858833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445460-G-T

38858841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445452-G-C

38858892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445401-G-A

38858920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445373-C-T

38858990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445220-G-A

38859069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445153-A-G

38859122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445117-G-A

38859167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445072-A-G

38859167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445072-A-T

http://identifiers.org/hco/13/GRCh38#38859175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53445064-C-A

38859175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445064-C-T

http://identifiers.org/hco/13/GRCh38#38859176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53445063-A-C

38859176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445063-A-G

38859178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445061-G-A

38859178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445061-G-T

38859189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445046-G-A

http://identifiers.org/hco/13/GRCh38#38859198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53445037-C-A

38859198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445037-C-T

38859241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53445001-A-G

38859246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444995-T-A

http://identifiers.org/hco/13/GRCh38#38859248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53444993-C-A

38859248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444993-C-G

38859248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444993-C-T

38859256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444985-T-C

38859293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53444939-A-G

38859371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53444861-C-T

38859389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53444843-C-T

38859395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53444837-G-A

38859428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53444804-G-C

38859428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53444804-G-T

38859437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53444795-G-A

38859488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53444744-C-G

38859592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: splice donor variant
orthologous variants: 53444640-T-C

38859632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444605-G-A

38859642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444595-A-G

38859668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444569-T-A

http://identifiers.org/hco/13/GRCh38#38859684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53444554-C-A

38859685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444553-A-G

38859685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444553-A-T

38859696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444542-A-G

http://identifiers.org/hco/13/GRCh38#38859948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53444361-A-C

38860185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444184-T-C

38860189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444180-G-A

38860238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444135-G-A

http://identifiers.org/hco/13/GRCh38#38860244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53444129-C-A

38860244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444129-C-T

38860245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444128-G-A

38860245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53444128-G-T

http://identifiers.org/hco/13/GRCh38#38860785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53443738-C-A

38860993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443651-G-T

38861241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443441-T-C

http://identifiers.org/hco/13/GRCh38#38861283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53443402-A-C

38861283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443402-A-G

38861283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443402-A-T

38861371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443327-T-G

38861379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443319-G-T

38861380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443318-T-C

38861380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443318-T-G

http://identifiers.org/hco/13/GRCh38#38861538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53443167-A-C

http://identifiers.org/hco/13/GRCh38#38861627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53443074-C-A

http://identifiers.org/hco/13/GRCh38#38861628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53443073-C-A

38861628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443073-C-T

38861675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443053-T-G

38861677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443051-G-A

38861677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443051-G-T

38861681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443047-T-C

38861687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443041-T-C

http://identifiers.org/hco/13/GRCh38#38861693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53443035-C-A

38861693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443035-C-T

38861727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53443011-T-A

38861752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442983-G-A

38864286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53442904-G-A

38864286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53442904-G-C

38864286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53442904-G-T

38864334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53442856-G-A

38864421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53442769-A-G

38864430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53442760-C-T

38864439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53442751-A-G

38864523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53442667-G-A

38864523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53442667-G-T

38864633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442557-G-A

38864633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442557-G-C

38864706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442502-G-T

38864710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442498-T-G

38864717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442491-T-A

38864717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442491-T-C

38864733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442477-G-A

38864733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442477-G-T

38865237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442340-C-T

38865272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53442316-A-G

38865651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441813-G-T

38865723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441723-T-G

38865788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441658-T-C

38865800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441649-A-G

38865832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441612-G-T

38866040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441458-T-A

38866041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441457-G-A

38866159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441370-T-C

38866183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441346-T-C

38866988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441116-G-A

38867034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441070-T-C

38867099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53441005-C-T

38867273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53440539-T-C

38867440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53440365-G-A

38867462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53440345-T-C

38868274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53440080-T-C

38868330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53439843-A-T

38868360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53439813-T-C

38868395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53439778-C-G

38868407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53439766-T-C

38868430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53439719-T-G

38868489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53439662-A-G

38868571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53439591-G-A

38868876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53438120-T-C

38868892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53438104-A-G

38868922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53438072-G-A

38868922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53438072-G-C

38868947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53438049-A-G

38869017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437983-A-G

38869017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437983-A-T

38869030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437970-C-T

38869173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437883-A-G

38869282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437755-A-G

38869529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437535-A-G

38869768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437263-C-G

38869770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437261-C-G

38869983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437109-A-G

38870078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53437031-A-G

http://identifiers.org/hco/13/GRCh38#38870125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53436996-C-A

38870290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53436421-G-T

38870425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53436288-T-C

38870536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53436215-A-G

38870644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53436105-C-T

38870666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53436086-T-G

38871027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53435063-C-T

38871091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53434993-A-G

38871164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53434943-T-G

38871165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53434942-A-T

38871224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53434878-G-T

38871301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53434797-G-A

38871357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53434756-G-T

38871521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53434608-C-T

38871547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53434589-A-T

38871809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53434101-T-G

38871979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433937-T-G

38872038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433870-G-A

38872090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433825-T-A

38872374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433676-A-T

38872556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433501-G-A

38872591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433491-G-A

38872591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433491-G-T

38872593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433489-G-A

38872624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433455-T-A

http://identifiers.org/hco/13/GRCh38#38872625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53433454-C-A

http://identifiers.org/hco/13/GRCh38#38872674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53433428-C-A

38872674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433428-C-G

38872674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433428-C-T

38872682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433420-A-G

http://identifiers.org/hco/13/GRCh38#38872692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53433410-C-A

38872862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53433250-C-G

38872940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433172-T-A

38872992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433125-G-A

38872992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53433125-G-T

http://identifiers.org/hco/13/GRCh38#38873029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53433076-C-A

http://identifiers.org/hco/13/GRCh38#38873077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53432895-C-A

38873077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432895-C-G

38873077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432895-C-T

38873084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432888-A-T

38873188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432769-T-C

38873376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432581-A-G

38873476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432479-T-C

38873560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432395-G-A

38873632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432171-A-G

38873643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432160-G-A

38873655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432148-T-A

38873661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432143-A-G

http://identifiers.org/hco/13/GRCh38#38873687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53432117-C-A

38873687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432117-C-G

38873694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432110-C-T

38873741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432065-G-C

38873782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53432024-T-C

38874092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431710-C-G

38874116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431685-A-T

38874135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431666-A-G

http://identifiers.org/hco/13/GRCh38#38874346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53431428-C-A

38874346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431428-C-G

38874346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431428-C-T

38874348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431426-G-A

38874348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431426-G-T

http://identifiers.org/hco/13/GRCh38#38874394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53431358-C-A

http://identifiers.org/hco/13/GRCh38#38874395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53431357-A-C

38874439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431227-C-G

38874571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53431097-G-T

38874629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431045-G-A

http://identifiers.org/hco/13/GRCh38#38874649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53431025-C-A

38874669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53431005-T-A

38874692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430982-T-A

http://identifiers.org/hco/13/GRCh38#38874697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53430977-A-C

38874740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430935-T-C

38874942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430732-A-G

38875008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430673-G-A

38875112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430577-A-G

38875206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430502-G-T

38875317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430420-A-G

38875332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430406-C-G

38875471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430262-T-C

38875550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430185-A-G

38875561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53430174-C-G

38875957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429846-A-G

http://identifiers.org/hco/13/GRCh38#38876104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53429716-C-A

38876104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: synonymous variant
orthologous variants: 53429716-C-T

38876384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: splice donor variant
orthologous variants: 53429451-T-C

38876385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429450-G-A

38876393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429442-T-C

38876415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429275-G-A

38876442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429231-T-A

38876442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429231-T-C

38876454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429219-A-T

http://identifiers.org/hco/13/GRCh38#38876458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53429215-A-C

38876458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429215-A-T

38876469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429182-T-A

38876469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429182-T-C

http://identifiers.org/hco/13/GRCh38#38876484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53429166-C-A

38876587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429065-T-G

38876655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429019-T-C

38876672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53429002-G-C

38876896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428784-C-T

38876957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428719-G-A

http://identifiers.org/hco/13/GRCh38#38876973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53428703-C-A

38876983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428693-T-G

38877011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428669-T-A

38877011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428669-T-G

38877065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428612-G-A

38877074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428598-C-T

38877092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428580-A-G

38877117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 53428552-G-A

38877117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 53428552-G-C

38877228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53428441-G-A

38877267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428395-A-G

38877267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428395-A-T

38877271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428391-T-C

38877282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428380-T-A

38877282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428380-T-C

38877287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428375-A-G

38877296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428367-G-A

38877298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428365-T-C

38877298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428365-T-G

http://identifiers.org/hco/13/GRCh38#38877302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53428361-C-A

38877312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428351-A-G

38877317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428332-G-C

38877321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428328-G-A

38877321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428328-G-C

38877326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428323-G-A

38877326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428323-G-T

38877332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428306-T-G

38877339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428299-T-C

38877339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428299-T-G

38877346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428292-A-G

38877351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428287-T-G

38877359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428283-T-A

38877359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428283-T-C

38877359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428283-T-G

38877362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428280-A-G

38877416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53428231-T-A

http://identifiers.org/hco/13/GRCh38#38877441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53428205-A-C

38877603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427968-A-T

38877730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427857-A-T

38877766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427821-A-G

38877802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427790-A-G

38877982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427639-G-C

38877982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427639-G-T

38877998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427625-G-T

38877999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427624-G-A

38877999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427624-G-T

38878022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427601-G-A

38878025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427598-G-A

38878025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427598-G-T

38878045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427578-T-C

38878061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427567-T-C

38878066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427562-T-C

38878093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427548-T-C

38878095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427546-T-C

38878097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427544-A-G

38878097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427544-A-T

38878099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427542-A-G

38878114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427528-T-C

http://identifiers.org/hco/13/GRCh38#38878117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53427525-C-A

38878259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53427385-A-G

38878723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427222-A-G

http://identifiers.org/hco/13/GRCh38#38878749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53427196-C-A

38878749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53427196-C-T

http://identifiers.org/hco/13/GRCh38#38878756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53427190-A-C

38878957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53426992-G-A

38878957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53426992-G-C

38878957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53426992-G-T

http://identifiers.org/hco/13/GRCh38#38879016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53426942-C-A

38879020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53426938-A-G

http://identifiers.org/hco/13/GRCh38#38879081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53426884-A-C

38879081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53426884-A-T

38879099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53426861-G-A

38879099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53426861-G-T

38879288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53426248-A-G

38879290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53426246-T-C

http://identifiers.org/hco/13/GRCh38#38879861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53424951-A-C

38879949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53424871-A-G

38880011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53424812-G-T

38880089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53424746-G-C

38880120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53424698-A-G

http://identifiers.org/hco/13/GRCh38#38880133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53424635-C-A

38880216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53424525-G-A

http://identifiers.org/hco/13/GRCh38#38880233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53424508-A-C

38880233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53424508-A-G

38880233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: intron variant
orthologous variants: 53424508-A-T

38880290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53424454-C-G

38880290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: synonymous variant
orthologous variants: 53424454-C-T

38880398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53424340-G-A

http://identifiers.org/hco/13/GRCh38#38880448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53424290-C-A

38880448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: synonymous variant
orthologous variants: 53424290-C-T

38880455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53424283-T-A

http://identifiers.org/hco/13/GRCh38#38880458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53424280-C-A

38880458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: synonymous variant
orthologous variants: 53424280-C-T

38880467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53424271-G-A

38880542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53424193-C-G

38880697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: 53424041-T-G

http://identifiers.org/hco/13/GRCh38#38880755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53423983-C-A

http://identifiers.org/hco/13/GRCh38#38880867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53423889-C-A

38880867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423889-C-G

38880885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423870-G-A

38880885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423870-G-T

38880989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423758-T-A

38881161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423587-G-T

http://identifiers.org/hco/13/GRCh38#38881171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53423577-C-A

38881171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423577-C-T

http://identifiers.org/hco/13/GRCh38#38881211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53423543-C-A

38881312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423451-G-A

38881357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423409-A-G

38881419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423348-G-A

38881503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423263-G-T

38881576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423200-G-T

38881607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423172-T-G

38881671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423109-A-G

38881688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53423092-C-T

38881949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53422849-G-T

38882025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53422767-A-G

38882026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53422766-G-C

38882030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53422762-A-G

38882457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53422105-A-T

38882523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53422063-C-G

38882523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53422063-C-T

http://identifiers.org/hco/13/GRCh38#38882569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53422012-C-A

38882569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53422012-C-T

38882622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53421955-A-G

38882924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53421678-A-G

38882966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53421652-G-T

38882976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53421642-G-T

38882995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53421623-C-G

38883035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53421582-T-A

38883380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53421321-A-G

http://identifiers.org/hco/13/GRCh38#38883384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53421317-A-C

38883645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53420865-G-T

38883741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53420781-T-C

38883744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53420778-T-C

38883784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53420731-A-G

38884488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53419353-C-T

http://identifiers.org/hco/13/GRCh38#38884548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53419302-A-C

38884671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53419057-G-T

38884686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53419042-C-T

38884787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53418955-G-C

38884817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53418932-G-T

38884839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53418910-A-G

38884846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53418906-G-A

38884861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53418891-G-A

38884919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: 53418842-A-G

http://identifiers.org/hco/13/GRCh38#38884979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25396
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53418793-A-C