3440070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 73236844-A-G

3440108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 73236810-A-G

3440114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 73236798-T-C

3440160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 73236757-A-G

http://identifiers.org/hco/17/GRCh38#3440454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73236437-C-A

3440454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73236437-C-T

3440524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73236384-G-A

3440524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73236384-G-T

3440528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73236380-G-C

3440528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73236380-G-T

3440542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73236365-A-G

3443157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73235584-A-T

3443178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, missense_variant
orthologous variants: 73235563-T-C

3443187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, missense_variant
orthologous variants: 73235554-A-T

3443265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, missense_variant
orthologous variants: 73235476-A-G

3443288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73235453-T-C

3443335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73235411-G-A

3443343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73235404-G-T

3444106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73235079-T-C

3446605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73234557-T-C

3446607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73234555-G-T

3447439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73232626-A-G

3447614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73232477-G-A

3447702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73232384-G-A

3447720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73232365-C-T

3448080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73232089-C-T

3448085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73232084-A-G

3448085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73232084-A-T

3448088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73232081-G-A

3448414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73231770-C-T

3448475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73231709-G-A

3448537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73231648-C-G

3448537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73231648-C-T

3448568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73231620-T-C

3448704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73231486-C-T

3448748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73231466-T-C

3448748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73231466-T-G

3448903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: synonymous variant
orthologous variants: 73231312-G-A

3449092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: synonymous variant
orthologous variants: 73231123-C-T

3449214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73231022-A-G

3449240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73230998-T-A

3449244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73230994-G-A

3449244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73230994-G-T

http://identifiers.org/hco/17/GRCh38#3449429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73230813-C-A

3462363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73227193-G-A

3462363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73227193-G-T

3462522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: missense variant
orthologous variants: 73227075-G-A

3462522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: missense variant
orthologous variants: 73227075-G-C

3462568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: missense variant
orthologous variants: 73227029-G-A

3462568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: missense variant
orthologous variants: 73227029-G-T

http://identifiers.org/hco/17/GRCh38#3462609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: -A-C

3462629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73226974-A-G

3462678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73226925-C-T

3465928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73226097-A-G

3466114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73225645-A-G

3466499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73225167-G-A

3466556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73225111-G-A

http://identifiers.org/hco/17/GRCh38#3466669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73225005-C-A

3467025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73224629-T-C

http://identifiers.org/hco/17/GRCh38#3467039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73224615-C-A

3467244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73224419-T-C

3467279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73224383-T-C

3468201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73223293-A-G

3468475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73223063-A-G

3468485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73223053-G-T

3468768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73222815-G-T

3469170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73222134-A-G

3469176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73222128-G-C

3469176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73222128-G-T

http://identifiers.org/hco/17/GRCh38#3469188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73222116-A-C

3469188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73222116-A-G

3469243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73222062-T-A

3469243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73222062-T-C

3469312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 73221989-A-G

3469331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73221970-T-C

3469334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73221967-A-G

3469375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73221931-T-A

3469375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73221931-T-C

3469376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73221930-A-G

3469376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73221930-A-T

3469382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73221924-A-G

3469394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73221916-T-A

3469394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73221916-T-C

3469413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73221897-A-G

3469413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73221897-A-T

3469468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73221846-T-C

3469639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73221689-G-A

3469710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73221621-G-A

3471546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220806-C-G

3471568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220784-G-A

3471568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220784-G-T

http://identifiers.org/hco/17/GRCh38#3471602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73220742-C-A

3471602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220742-C-T

http://identifiers.org/hco/17/GRCh38#3471609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73220735-C-A

3471609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220735-C-T

3471646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220693-C-T

http://identifiers.org/hco/17/GRCh38#3471748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73220592-C-A

3471766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220574-G-A

3471766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220574-G-C

3471837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220497-C-T

3471873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220433-G-A

http://identifiers.org/hco/17/GRCh38#3471896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73220392-C-A

3471896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220392-C-T

3471900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220388-C-T

http://identifiers.org/hco/17/GRCh38#3471915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73220373-C-A

3471915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220373-C-T

3471928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220360-A-T

3471940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220346-G-A

3471940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220346-G-T

http://identifiers.org/hco/17/GRCh38#3471960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73220321-C-A

3471960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220321-C-T

http://identifiers.org/hco/17/GRCh38#3472047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73220235-C-A

3472047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220235-C-T

http://identifiers.org/hco/17/GRCh38#3472161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73220122-C-A

3472161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220122-C-T

3472167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73220114-G-A

3472297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73219986-G-A

3472419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73219684-T-C

http://identifiers.org/hco/17/GRCh38#3472422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73219681-C-A

3472422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73219681-C-T

3472443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73219630-T-A

3472443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73219630-T-C

3472626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73219457-G-A

3472670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73219405-T-C

3472925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73219204-T-G

http://identifiers.org/hco/17/GRCh38#3473138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73218756-C-A

3473328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73218547-C-T

3473856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73217956-A-G

3474005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73217770-G-A

3474082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73217693-G-T

3474107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73217669-G-T

3474227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73217558-A-G

3474369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73217419-G-A

3474494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73217295-T-C

3474609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73217193-T-G

3474860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73216957-G-A

3475049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73216772-A-T

3475257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73216507-T-A

3475365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73216357-G-T

3475718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73215717-G-T

http://identifiers.org/hco/17/GRCh38#3475722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#73215713-C-A

3475722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73215713-C-T

3475744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73215690-A-T

3475913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73215566-G-A

3475913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73215566-G-T

3476022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73215447-A-T

3476283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 73215191-C-T

http://identifiers.org/hco/17/GRCh38#3476546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73214932-A-C

3476546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73214932-A-G

3476564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73214914-C-T

3476672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73214833-G-C

3476727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73214766-G-C

3480008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73213901-T-C

3480082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73213838-T-C

http://identifiers.org/hco/17/GRCh38#3481515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73213190-C-A

3481515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73213190-C-T

3481805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 73212903-T-A

3481805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 73212903-T-G

3481949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73212790-G-A

3481949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73212790-G-C

3482308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73212492-C-T

3483296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73210901-T-C

3483354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73210860-T-C

3483354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73210860-T-G

3483358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73210856-G-A

3483358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73210856-G-T

http://identifiers.org/hco/17/GRCh38#3486615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73210149-C-A

http://identifiers.org/hco/17/GRCh38#3486934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73208048-C-A

3487077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73208163-T-A

3487274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73208350-T-C

3487274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73208350-T-G

3488156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73205092-T-A

3488156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73205092-T-C

http://identifiers.org/hco/17/GRCh38#3489102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73204555-C-A

3489102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73204555-C-T

3489203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73204470-A-G

3489203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, undefined
orthologous variants: 73204470-A-T

3489258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, stop_gained
orthologous variants: 73204418-C-T

3489343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 73204333-G-A

3489343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 73204333-G-T

3489440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73204040-T-G

3490188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73202185-C-T

3490702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73201700-A-G

3494872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73198508-A-G

3495119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73198294-T-C

3495224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73198214-C-G

3495224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73198214-C-T

3495228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73198210-G-A

3495228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73198210-G-C

3495239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73198199-G-A

3495274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73198164-C-T

3495979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73197698-G-A

3496021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73197645-G-A

3496038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73197628-C-T

3496116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73197553-G-A

3498736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73196620-G-A

3498751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73196605-G-T

3498816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73196536-T-C

3499246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73196097-T-A

3499246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73196097-T-G

3499247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73196096-A-G

3499247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73196096-A-T

3502455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73195871-T-C

3502685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73195659-C-T

3502785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73195565-G-A

3502785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73195565-G-T

3503015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73195364-G-T

3503173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 73195215-T-C

3505630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73192842-G-A

3506225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73192572-G-A

3506506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73192184-A-G

3506507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73192183-T-C

3507179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73191722-G-A

3507179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73191722-G-C

3510410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73191282-G-A

3510498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: intron variant
orthologous variants: 73191196-G-T

3510525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73191169-T-A

3510551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73191146-A-G

http://identifiers.org/hco/17/GRCh38#3510792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73190905-C-A

http://identifiers.org/hco/17/GRCh38#3510806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73190891-C-A

3511044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190673-T-C

3511059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190658-C-T

http://identifiers.org/hco/17/GRCh38#3511062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73190655-C-A

3511062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190655-C-T

3511072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190645-A-G

3511122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190595-G-A

3511122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190595-G-T

3511152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190564-G-A

3511152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190564-G-C

3511152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190564-G-T

3511173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190554-G-A

3511173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190554-G-T

3511185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190542-G-T

3511194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190533-T-C

3511290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190436-T-G

3511402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190356-C-G

http://identifiers.org/hco/17/GRCh38#3511446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73190325-C-A

3511446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190325-C-T

http://identifiers.org/hco/17/GRCh38#3511455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73190316-A-C

3511455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190316-A-G

3511501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190270-G-A

3511501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190270-G-T

3511588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73190172-G-T

http://identifiers.org/hco/17/GRCh38#3511654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73190104-C-A

http://identifiers.org/hco/17/GRCh38#3511757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73190012-A-C

3511772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189997-T-G

3511781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189988-G-A

3511781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189988-G-C

3511781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189988-G-T

3511783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189986-G-A

3511783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189986-G-C

3511783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189986-G-T

3511897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189958-A-G

3512095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189799-A-T

http://identifiers.org/hco/17/GRCh38#3512097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73189797-A-C

3512097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189797-A-G

3512141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189753-T-A

3512178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189712-C-T

3512239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189654-G-A

3512291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189596-T-C

3512329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189558-A-G

http://identifiers.org/hco/17/GRCh38#3512332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73189555-C-A

3512332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189555-C-G

3512332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189555-C-T

3512378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189498-T-C

3512389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189487-A-G

3512419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189457-C-T

3512481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189405-G-T

3512502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189384-A-G

3512509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189377-G-T

3512622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189234-A-T

3512635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189215-T-C

3512671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73189179-A-T

http://identifiers.org/hco/17/GRCh38#3512969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188900-C-A

3513019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188865-T-C

3513047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188834-A-G

3513111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188776-G-A

3513111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188776-G-T

3513153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188734-A-G

http://identifiers.org/hco/17/GRCh38#3513164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188723-C-A

3513164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188723-C-T

3513223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188661-G-A

3513223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188661-G-T

http://identifiers.org/hco/17/GRCh38#3513270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188614-A-C

3513270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188614-A-G

http://identifiers.org/hco/17/GRCh38#3513348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188542-C-A

3513348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188542-C-G

3513348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188542-C-T

http://identifiers.org/hco/17/GRCh38#3513371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188521-C-A

3513390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188502-T-A

3513390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188502-T-C

http://identifiers.org/hco/17/GRCh38#3513426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188464-C-A

http://identifiers.org/hco/17/GRCh38#3513428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188462-C-A

3513428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188462-C-T

http://identifiers.org/hco/17/GRCh38#3513430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188460-C-A

3513430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188460-C-G

3513430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188460-C-T

http://identifiers.org/hco/17/GRCh38#3513476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188421-C-A

3513497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73188393-G-T

http://identifiers.org/hco/17/GRCh38#3513597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188291-C-A

3513649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, undefined
orthologous variants: 73188252-A-G

3513649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, undefined
orthologous variants: 73188252-A-T

3513792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, undefined
orthologous variants: 73188128-G-A

3513792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, undefined
orthologous variants: 73188128-G-C

3513792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, undefined
orthologous variants: 73188128-G-T

http://identifiers.org/hco/17/GRCh38#3513799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30705
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#73188121-C-A