http://identifiers.org/hco/9/GRCh38#131289530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31985366-C-A

131289530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31985366-C-G

131289575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31985422-G-A

131289575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31985422-G-T

http://identifiers.org/hco/9/GRCh38#131289668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31985520-C-A

131289668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31985520-C-T

131289711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 31985563-G-A

131289711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 31985563-G-T

131289790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 31985643-G-A

131289790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 31985643-G-T

http://identifiers.org/hco/9/GRCh38#131290082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31985908-C-A

131290264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31986090-T-C

131290285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31986111-G-A

http://identifiers.org/hco/9/GRCh38#131290417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31986243-C-A

131290417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31986243-C-T

131290461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31986287-G-A

131290461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31986287-G-C

131290461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31986287-G-T

131290465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31986298-C-T

http://identifiers.org/hco/9/GRCh38#131290597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31986418-C-A

131290597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31986418-C-T

http://identifiers.org/hco/9/GRCh38#131290852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31986646-C-A

http://identifiers.org/hco/9/GRCh38#131290991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31986764-C-A

131291037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31986810-T-C

131291127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31986890-G-A

131291164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31986928-T-G

131291196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31986960-G-A

131291196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31986960-G-T

131291233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31986997-G-T

131291405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31987056-C-T

131291427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31987076-C-G

131291449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987099-T-C

131291459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987113-G-A

http://identifiers.org/hco/9/GRCh38#131291492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31987145-C-A

131291492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987145-C-G

131291492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987145-C-T

131291497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987150-A-G

http://identifiers.org/hco/9/GRCh38#131291541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31987193-C-A

131291541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987193-C-G

131291541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987193-C-T

131291583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987199-G-T

131291967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987349-C-T

131292153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987475-C-T

131292337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987645-C-T

131292451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987730-G-A

131292560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987792-C-G

131292634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987857-G-A

131292715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987932-G-A

131292715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987932-G-T

http://identifiers.org/hco/9/GRCh38#131292764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31987981-C-A

131292764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31987981-C-T

131292788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 31988006-G-T

131292796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31988016-G-A

131292807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 31988027-C-T

131292808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31988028-A-G

131292828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31988046-T-G

131292861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31988078-C-T

http://identifiers.org/hco/9/GRCh38#131293065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31988321-C-A

131293065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31988321-C-T

http://identifiers.org/hco/9/GRCh38#131293095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31988352-C-A

131293095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31988352-C-T

http://identifiers.org/hco/9/GRCh38#131293211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31988449-C-A

131293211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31988449-C-G

131293626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989585-C-T

131293666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989620-A-G

131293790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989715-T-C

http://identifiers.org/hco/9/GRCh38#131293821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31989730-C-A

131293855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989762-A-T

131293860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989767-G-A

131293860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989767-G-C

131293894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989800-G-A

131293894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989800-G-T

131293904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989810-G-A

131294051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31989910-G-A

131294451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31990241-G-A

131294466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31990253-C-G

131294558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31990341-A-T

131294593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31990371-T-C

131296688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31993573-G-A

131297194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31994028-T-C

131297282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31994116-C-T

131297738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31995067-A-G

131297779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31995109-C-T

131297954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31995274-G-A

131298331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31995636-C-T

131298499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31995740-C-G

http://identifiers.org/hco/9/GRCh38#131298677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31995872-A-C

131298831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31996017-G-A

131298831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31996017-G-C

http://identifiers.org/hco/9/GRCh38#131299088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31996268-C-A

131299192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31996377-G-A

131299192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31996377-G-C

131299727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31996779-C-T

131299783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31996831-G-A

131304171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31997561-C-T

131304217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31997610-C-G

131304283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31997675-C-G

131304733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31997984-T-C

131307780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999473-A-G

131307826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999513-G-A

131307826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999513-G-T

131307834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999524-A-G

131307836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999526-G-T

131307837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999527-G-A

131307837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999527-G-C

131307837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999527-G-T

131307844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999534-A-T

131307848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999545-G-A

131307848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999545-G-T

131307853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999550-T-G

http://identifiers.org/hco/9/GRCh38#131307875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31999572-C-A

131307898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31999596-A-G

http://identifiers.org/hco/9/GRCh38#131307996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31999694-C-A

131307996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 31999694-C-T

http://identifiers.org/hco/9/GRCh38#131308003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31999701-C-A

131308003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31999701-C-G

131308003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31999701-C-T

http://identifiers.org/hco/9/GRCh38#131308209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31999907-C-A

131308209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 31999907-C-T

131308225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31999923-C-G

131308225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31999923-C-T

http://identifiers.org/hco/9/GRCh38#131308251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31999949-C-A

131308251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 31999949-C-T

131308485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000115-A-G

http://identifiers.org/hco/9/GRCh38#131308539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32000165-C-A

131308539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000165-C-G

131308539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000165-C-T

http://identifiers.org/hco/9/GRCh38#131308540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32000166-C-A

http://identifiers.org/hco/9/GRCh38#131308629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32000262-A-C

131308629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000262-A-G

131308684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000315-G-A

131308684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000315-G-T

131308741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000353-G-A

http://identifiers.org/hco/9/GRCh38#131308743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32000355-C-A

131308743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000355-C-G

131308743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000355-C-T

http://identifiers.org/hco/9/GRCh38#131308784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32000395-C-A

131308786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000397-G-A

131308786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000397-G-T

131308792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000403-G-A

131308792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000403-G-C

131308792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000403-G-T

131308806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000415-G-A

131308806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000415-G-C

131308806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000415-G-T

http://identifiers.org/hco/9/GRCh38#131309110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32000692-C-A

131309149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000731-C-T

131309199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32000781-G-A

131309357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32000887-G-A

131309357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32000887-G-T

131309616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32001116-T-C

131309630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32001130-T-A

131309630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32001130-T-C

131309770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32001202-G-A

131310101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32001502-C-T

http://identifiers.org/hco/9/GRCh38#131310228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32001614-A-C

131310228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32001614-A-T

131311281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003240-A-G

131311402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003389-A-G

131311422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003411-G-A

131311611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003545-T-C

131311676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003600-A-G

131311696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003621-G-A

131311696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003621-G-T

131311706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003631-C-T

131311754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003670-G-A

131311777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003694-G-A

131311777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003694-G-C

131311814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32003728-T-C

131313139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32003929-G-A

131313139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32003929-G-T

http://identifiers.org/hco/9/GRCh38#131313438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32004209-C-A

131313438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32004209-C-G

131313438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32004209-C-T

131320250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32011417-G-A

131320281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32011441-G-T

131320348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32011494-C-T

131320365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32011513-A-G

131320397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32011544-G-A

131331016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32017947-G-A

131331365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32018219-C-G

131331416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32018273-G-A

131331502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32018359-G-A

131331535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32018395-G-A

131331535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32018395-G-T

131331672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32018535-G-A

131331793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32018665-C-T

131334636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32019701-G-A

131334636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32019701-G-C

131334653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32019718-T-C

131334659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32019724-T-C

131334797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32019802-C-T

131335235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32020203-G-C

131335376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32020356-C-T

131335524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32020453-G-A

131335541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32020469-G-A

131335555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32020483-C-T

131335584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32020493-T-C

131336070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32020810-T-C

131336070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32020810-T-G

131336673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32021250-T-C

131336695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32021264-T-C

131336775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32021338-G-A

131336775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32021338-G-C

131336865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32021391-G-A

131337483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32021854-T-C

131337515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32021886-T-C

131337611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32021984-G-A

131337611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28174
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32021984-G-T